Copy number variation (CNV) variant
Evidence from:
primary |
all sources
Related entities (2)
| Subject | Relation | Object | p-value | Evidence |
|---|---|---|---|---|
| Copy number variation (CNV) | risk_factor_for | psychiatric disorders | — | 1 |
| de novo variant | associated_with | Copy number variation (CNV) | — | 1 |
Mentioned in (4)
Papers in which this entity is mentioned.
- Comprehensive analysis of structural variants in breast cancer genomes using single-molecule sequencing. (2020)
- The impact of structural variation on human gene expression. (2017)
- Copy number variation: what is it and what has it told us about child psychiatric disorders? (2013)
- CNVs: harbingers of a rare variant revolution in psychiatric genetics. (2012)
Merged raw entities (2)
All extracted name/type variants the normalize job merged into this entity. Use this to spot wrong merges, or aliases that should be split off.
| Raw name | Type | Papers | Mentions |
|---|---|---|---|
| copy number variation (cnv) | variant | 4 | 4 |
| rare cnv alleles | variant | — | — |