Target Copy Number Variation Details
- DGV Version
- Release date: 2016-05-15, GRCh GRCh38
Target Variation ID |
Location |
CNV Subtype |
Genes |
nsv1054778 |
Chr14:21294781 - 21334420 on Build GRCh38 |
Gain |
RPGRIP1
|
Product Details
- Assay Reference Genome
Location
Chr.14:21312442 on build GRCh38
- Cytoband
- 14q11.2
- Species
- Homo sapiens
- Variation Type
- Copy Number
Additional Information
Target Gene Details
- Entrez Gene ID
- 57096
- Gene Symbol
- RPGRIP1
- Gene Name
- retinitis pigmentosa GTPase regulator interacting protein 1
- Gene Aliases
- CORD13, LCA6, RGI1, RGRIP, RPGRIP, RPGRIP1d
- Location
- Chr.14:21287977-21351316 on build GRCh38
- Assay Gene Location
- Overlaps Intron 8 - Intron 9
Target Copy Number Variation Details
- DGV Version
- Release date: 2016-05-15, GRCh GRCh38
Target Variation |
Location |
CNV Subtype |
Genes |
nsv1054778 |
Chr14:21294781 - 21334420 on Build GRCh38 |
Gain |
RPGRIP1
|
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