Target Copy Number Variation Details
- DGV Version
- Release date: 2016-05-15, GRCh GRCh38
Target Variation ID |
Location |
CNV Subtype |
Genes |
esv2661363 |
ChrX:31137680 - 31139688 on Build GRCh38 |
Deletion |
DMD
|
Product Details
- Assay Reference Genome
Location
Chr.X:31139020 on build GRCh38
- Cytoband
- Xp21.2
- Species
- Homo sapiens
- Variation Type
- Copy Number
Additional Information
Target Gene Details
- Entrez Gene ID
- 1756
- Gene Symbol
- DMD
- Gene Name
- dystrophin
- Gene Aliases
- BMD, CMD3B, DXS142, DXS164, DXS206, DXS230, DXS239, DXS268, DXS269, DXS270, DXS272, MRX85
- Location
- Chr.X:31119219-33339609 on build GRCh38
- Assay Gene Location
- Within Intron 85
Target Copy Number Variation Details
- DGV Version
- Release date: 2016-05-15, GRCh GRCh38
Target Variation |
Location |
CNV Subtype |
Genes |
esv2661363 |
ChrX:31137680 - 31139688 on Build GRCh38 |
Deletion |
DMD
|
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