Target Copy Number Variation Details
- DGV Version
- Release date: 2016-05-15, GRCh GRCh38
Target Variation ID |
Location |
CNV Subtype |
Genes |
esv32898 |
Chr4:41744516 - 41746501 on Build GRCh38 |
Gain |
PHOX2B
|
Product Details
- Assay Reference Genome
Location
Chr.4:41745074 on build GRCh38
- Cytoband
- 4p13
- Species
- Homo sapiens
- Variation Type
- Copy Number
Additional Information
Target Gene Details
- Entrez Gene ID
- 8929
- Gene Symbol
- PHOX2B
- Gene Name
- paired like homeobox 2b
- Gene Aliases
- NBLST2, NBPhox, PMX2B
- Location
- Chr.4:41744082-41748970 on build GRCh38
- Assay Gene Location
- Within Exon 3
Target Copy Number Variation Details
- DGV Version
- Release date: 2016-05-15, GRCh GRCh38
Target Variation |
Location |
CNV Subtype |
Genes |
esv32898 |
Chr4:41744516 - 41746501 on Build GRCh38 |
Gain |
PHOX2B
|
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