CNV
Term · Oncology and biomedicine · MLC-T-ONC-001867
A variation in the number of copies of a particular sequence of DNA present in the genome of an individual. CNVs include insertions, deletions, and duplications of segments of DNA. They account for a significant number of the genetic variations between individuals. CNVs may also be associated with specific traits or disorders. Also called copy number variant.
| Identifier | MLC-T-ONC-001867 |
|---|---|
| Field | Oncology and biomedicine |
| Expansions | copy number variant |
| References | NCI Dictionary of Genetics Terms |
Record as JSON
{
"id": "MLC-T-ONC-001867",
"term": "CNV",
"field": "Oncology and biomedicine",
"definition": "A variation in the number of copies of a particular sequence of DNA present in the genome of an individual. CNVs include insertions, deletions, and duplications of segments of DNA. They account for a significant number of the genetic variations between individuals. CNVs may also be associated with specific traits or disorders. Also called copy number variant.",
"expansions": [
"copy number variant"
],
"references": [
"NCI Dictionary of Genetics Terms"
],
"url": "https://mlchart.com/terminology/oncology/cnv/"
}
Record 5,044 of 17,721 in Oncology and biomedicine terminology (MLC-0111). Request the full dataset.