Target Copy Number Variation Details
- DGV Version
- Release date: 2016-05-15, GRCh GRCh38
Target Variation ID |
Location |
CNV Subtype |
Genes |
nsv831278 |
Chr8:31059468 - 31213390 on Build GRCh38 |
Gain |
WRN
|
Product Details
- Assay Reference Genome
Location
Chr.8:31072457 on build GRCh38
- Cytoband
- 8p12
- Species
- Homo sapiens
- Variation Type
- Copy Number
Additional Information
For this assay, SNP(s) [rs75027493] are located under a primer or probe sequence. To help evaluate the possible impact of a given SNP on your experiment, please refer to the 1000 Genomes and NCBI dbSNP databases. A higher minor allele frequency in your study population represents a higher risk to assay performance.
Target Gene Details
- Entrez Gene ID
- 7486
- Gene Symbol
- WRN
- Gene Name
- Werner syndrome RecQ like helicase
- Gene Aliases
- RECQ3, RECQL2, RECQL3
- Location
- Chr.8:31033262-31173761 on build GRCh38
- Assay Gene Location
- Within Intron 7
Target Copy Number Variation Details
- DGV Version
- Release date: 2016-05-15, GRCh GRCh38
Target Variation |
Location |
CNV Subtype |
Genes |
nsv831278 |
Chr8:31059468 - 31213390 on Build GRCh38 |
Gain |
WRN
|
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