Skip to main content
DNA Labs India

IgVH Hypermuation Analysis Confirmatory Test

DNA Labs India | ISO 9001:2015 Certified

IgVH Hypermuation Analysis Confirmatory Test

Short Name: IgVH Mutation Test

Also known as: IgVH Mutation Status Test, IGHV Hypermutation Analysis, Immunoglobulin Variable Heavy Chain Mutation Test

IgVH Hypermuation Analysis Confirmatory Test test available at DNA Labs India for ₹25,000. Uses Next Generation Sequencing (NGS) on Whole Blood samples. Results in Report available within 10 days of sample collection.. Free home collection in 300+ cities across India.

Genetic AnalysisAdults🏠 Home Collection

🩺 Medically Reviewed By

Overview

The purpose of the IgVH Hypermutation Analysis Confirmatory Test is to determine the mutational status of the IgVH gene in lymphocytes. This information helps in confirming the diagnosis of CLL or SLL, assessing prognosis, and making informed decisions about treatment. It also detects clonal expansions that may be missed by other methods.

Test Code
856
Price
₹25,000
Sample Type
Whole Blood
Result Time
Report available within 10 days of sample collection.
Fasting Required
No
Method
Next Generation Sequencing (NGS)
Step 1

Sample Collection

No special preparation required. Inform your doctor about any medications or health conditions.

Method: Venipuncture

Step 2

Laboratory Analysis

A blood sample will be drawn from a vein in your arm using standard venipuncture technique by a trained phlebotomist.

Step 3

Report Delivery

Apply pressure to the puncture site and keep it bandaged. Resume normal activities immediately.

Timeline: Report available within 10 days of sample collection.

Patient Instructions

1
Before the Test:Consult with your hematologist or oncologist for a referral. No fasting or special preparation is required for this test.
2
During the Test:The test involves a simple blood draw, which is quick and performed by trained phlebotomists in a clinical setting or via home collection.
3
After the Test:Results will be available in 10 days. Discuss the findings with your doctor to understand the implications for your diagnosis and treatment plan.

About This Test

Who Should Get This Test

The purpose of the IgVH Hypermutation Analysis Confirmatory Test is to determine the mutational status of the IgVH gene in lymphocytes. This information helps in confirming the diagnosis of CLL or SLL, assessing prognosis, and making informed decisions about treatment. It also detects clonal expansions that may be missed by other methods.

How to Prepare

  • Collect 4 mL (2 mL min.) whole blood in 1 Lavender top (EDTA) tube.
  • Ship refrigerated. DO NOT FREEZE.
  • Label tube with patient name and details.

Doctor's Notes

Reviewed by — MBBS, MD (Pathology) · Reg. No. 21521

"The IgVH Hypermutation status is a key prognostic marker in CLL, helping to guide treatment decisions."

Last medically reviewed: September 7, 2026

Test Parameters & Specifications

Sample TypeWhole Blood
Sample Volume4 mL (2 mL min.)
ContainerLavender top (EDTA) tube
Collection MethodVenipuncture

Sample Stability

Room Temperature6 hours
Refrigerator1 week
FrozenNot Applicable
Sample Rejection Criteria:
  • Hemolyzed sample
  • Insufficient volume (<2 mL)
  • Incorrect container type
  • Improper labeling or missing details

Understanding Your Results

Results indicate the mutational status of the IgVH gene. Mutated IgVH is associated with a better prognosis in CLL, while unmutated indicates a more aggressive disease. Clonal expansion findings may require further evaluation.
📊

Typically favorable prognosis, slower disease progression. Often responds better to treatment.

Status: Mutated IgVH

📊

Often associated with more aggressive disease, poorer outcome, and may require intensive therapy.

Status: Unmutated IgVH

📊

Indicates complex disease biology, which may influence treatment decisions and monitoring.

Status: Bi-clonal/Multi-clonal expansion

⚠️ When to Consult a Doctor:

If you experience symptoms such as enlarged lymph nodes, fatigue, weight loss, or night sweats, or if your test results are abnormal, consult your oncologist immediately for further evaluation and management.

Limitations

  • Cannot detect all genetic mutations.
  • Results should be correlated with clinical findings.
  • Limited to IgVH analysis; other markers may be needed for comprehensive diagnosis.

Risks & Considerations

  • Minor pain or bruising at the blood draw site.
  • Very rare risk of infection or fainting.

Interfering Factors

  • Hemolyzed or lipemic samples may affect results.
  • Insufficient sample volume.
  • Contamination during sample processing.

Compare With Similar Tests

TestIgVH Hypermuation Analysis Confirmatory Test
ComparisonIgVH Hypermuation Analysis Confirmatory Test

Frequently Asked Questions

What is the IgVH Hypermutation Analysis Confirmatory Test?
It is a genetic test that analyzes the mutational status of the IgVH gene in lymphocytes to help diagnose and assess prognosis in CLL and SLL.
Who should take this test?
Individuals with symptoms of CLL/SLL, those already diagnosed, or patients needing prognostic assessment for treatment planning.
How is the test performed?
A blood sample is collected in an EDTA tube and analyzed using next-generation sequencing (NGS) to detect IgVH mutations.
What does a mutated IgVH result mean?
Mutated IgVH (less than 98% identity to germline) generally indicates a better prognosis and slower disease progression in CLL.
What does an unmutated IgVH result mean?
Unmutated IgVH (98% or more identity) is often associated with a more aggressive form of CLL and poorer outcome.
Is there any preparation required before the test?
No special preparation is needed. Inform your doctor about any medications, but fasting is not required.
How long does it take to get the results?
Results are typically available within 10 days of sample collection.
What is the cost of the test?
The cost of the IgVH Hypermutation Analysis Confirmatory Test is INR 25000.0, with free home collection available for online bookings.
Is home collection available for this test?
Yes, DNA Labs India offers free home sample collection across many cities in India for this test.
Can this test detect all types of CLL?
It specifically analyzes IgVH mutation status, which is a key marker in CLL, but may not detect all genetic variations; other tests might be needed.
What are the limitations of this test?
It cannot detect all mutations, and results should be interpreted alongside clinical findings. It focuses solely on IgVH analysis.
How does this test differ from other genetic tests for CLL?
It uses NGS for higher sensitivity in detecting clonal expansions, unlike Sanger sequencing, and provides specific prognostic information on IgVH status.
Worried about the process? Our certified phlebotomists collect thousands of samples every month across India. The process takes under 5 minutes and is virtually painless. Questions? Message us on WhatsApp — we're here 7 days a week.

Related Tests

For Hospitals & Clinics

Reference Laboratory Services

We serve as a reference laboratory for hospitals and clinics across India. Send samples from your facility with same-day pickup, priority processing, and results delivered through our online portal. Competitive institutional pricing available.

LIMS Integration

Your Data Privacy

Your medical data is protected under Indian law.

Stored in India: All patient records are stored on servers located in India. No data is transferred outside the country.

DPDP Act Compliant: Under the Digital Personal Data Protection Act 2023, you can request deletion of your records at any time by contacting support.

Book Your Test

Enter your details and we'll connect you within 15 minutes.

🧬

Quick Connect

Enter your mobile number and we’ll connect you with the team.

+91

✅ Connecting you now...

🔒 Your number is used to respond to this request.