| Preferred Name |
Copy number variation |
| Synonyms |
CNV deletion Copy number variant CNV duplication Complex CNV CNV insertion / amplification |
| ID |
http://edamontology.org/topic_3958 |
| Created in |
1.25 |
| hasDefinition |
A DNA structural variation, specifically a duplication or deletion event, resulting in sections of the genome to be repeated, or the number of repeats in the genome to vary between individuals. |
| hasHumanReadableId |
Copy_number_variation |
| hasNarrowSynonym |
CNV deletion Copy number variant CNV duplication Complex CNV CNV insertion / amplification |
| label |
Copy number variation |
| prefixIRI |
topic_3958 |
| prefLabel |
Copy number variation |
| seeAlso | |
| subClassOf |