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Chromosome 21 Test

DNA Labs India | ISO 9001:2015 Certified

Chromosome 21 Test

Short Name: Chromosome 21 Test

Also known as: Down syndrome test, Trisomy 21 test, Chromosome 21 analysis

Chromosome 21 Test test available at DNA Labs India for ₹5,500. Uses FISH on Amniotic fluid / Chorionic villi / Cord blood samples. Results in 3-4 days. Free home collection in 300+ cities across India.

OncologyAll ages, including prenatal and postnatal🏠 Home Collection

🩺 Medically Reviewed By

Overview

The purpose of the Chromosome 21 test is to diagnose abnormalities in chromosome 21, such as trisomy 21 (Down syndrome), to enable early intervention, genetic counseling, and appropriate medical management.

Test Code
2966
Price
₹5,500
Sample Type
Amniotic fluid / Chorionic villi / Cord blood
Result Time
3-4 days
Fasting Required
No
Method
FISH
Step 1

Sample Collection

A doctor's prescription is required for the Chromosome 21 test, except in cases of surgery, pregnancy, or travel abroad. No fasting is needed.

Method: Invasive procedures such as amniocentesis, chorionic villus sampling (CVS), or cord blood collection

Step 2

Laboratory Analysis

Sample collection is performed via invasive procedures like amniocentesis, CVS, or cord blood draw by a healthcare professional.

Step 3

Report Delivery

Post-collection, samples are handled with care and transported under appropriate conditions (ambient or cool pack) to the laboratory for analysis.

Timeline: 3-4 days

Patient Instructions

1
Before the Test:Obtain a doctor's prescription. Inform the healthcare provider about any medical history or pregnancy status.
2
During the Test:The test involves sample collection through amniocentesis, CVS, or cord blood draw, which may cause mild discomfort but is generally safe.
3
After the Test:Results are typically available in 3-4 days. Follow up with your doctor for interpretation and next steps.

About This Test

Who Should Get This Test

The purpose of the Chromosome 21 test is to diagnose abnormalities in chromosome 21, such as trisomy 21 (Down syndrome), to enable early intervention, genetic counseling, and appropriate medical management.

How to Prepare

  • Use sterile containers or sodium heparin vacutainers as specified.
  • Ensure proper labeling and transport under ambient or cool conditions.
  • Follow aseptic techniques to avoid contamination.

Doctor's Notes

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

"Early diagnosis of Chromosome 21 abnormalities is crucial for timely intervention and management, especially in conditions like Down syndrome."

Last medically reviewed: September 7, 2026

Test Parameters & Specifications

Sample TypeAmniotic fluid / Chorionic villi / Cord blood
ContainerSterile container / Sterile Normal Saline Container / Sodium heparin Vacutainer (2ml)
Collection MethodInvasive procedures such as amniocentesis, chorionic villus sampling (CVS), or cord blood collection

Understanding Your Results

Results from the Chromosome 21 test indicate the presence or absence of abnormalities. A normal result shows two copies of chromosome 21, while an abnormal result may reveal trisomy 21 or other structural changes.
📊

Normal

Two copies of chromosome 21 detected, no abnormalities.

📊

Abnormal (e.g., Trisomy 21)

Three copies of chromosome 21 detected, indicating Down syndrome or related condition.

⚠️ When to Consult a Doctor:

Consult a doctor if you or your child exhibit symptoms such as intellectual disability, distinct facial features, heart defects, or developmental delays, or if prenatal screening suggests a risk for chromosome 21 abnormalities.

Risks & Considerations

  • Potential risks from invasive procedures include infection, bleeding, or miscarriage in prenatal cases, though rare.

Frequently Asked Questions

What is the Chromosome 21 test?
The Chromosome 21 test is a diagnostic test that analyzes chromosome 21 for abnormalities, such as trisomy 21 (Down syndrome), using methods like FISH.
Why is the Chromosome 21 test done?
It is done to diagnose chromosome 21 abnormalities, enabling early intervention, genetic counseling, and management of conditions like Down syndrome.
What are the symptoms of Chromosome 21 abnormalities?
Symptoms include intellectual disability, distinct facial features, short stature, poor muscle tone, heart defects, hearing problems, and developmental delays.
How is the Chromosome 21 test performed?
The test involves collecting samples such as amniotic fluid, chorionic villi, or cord blood, which are then analyzed using FISH to detect chromosome 21 abnormalities.
What is the cost of the Chromosome 21 test at DNA Labs India?
The test costs INR 5500, with free home sample collection available across India.
Is home collection available for the Chromosome 21 test?
Yes, DNA Labs India offers free home sample collection for online bookings in numerous cities across India.
How long does it take to get results for the Chromosome 21 test?
Results are usually available within 3-4 days after sample collection.
Is fasting required for the Chromosome 21 test?
No, fasting is not required for this test.
What are the risks associated with the Chromosome 21 test?
Risks are minimal but may include infection, bleeding, or miscarriage in prenatal cases due to invasive sample collection procedures.
Who should get the Chromosome 21 test?
Individuals with symptoms of chromosome 21 abnormalities, prenatal screening indications, or a family history of genetic disorders should consider testing.
What is the accuracy of the Chromosome 21 test?
The test using FISH is highly accurate for detecting chromosome 21 abnormalities, but accuracy may depend on sample quality and laboratory standards.
How can I book the Chromosome 21 test?
You can book the test online through DNA Labs India's website or contact them via phone or WhatsApp for assistance.
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.

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