Target Copy Number Variation Details
- DGV Version
- Release date: 2016-05-15, GRCh GRCh38
Target Variation ID |
Location |
CNV Subtype |
Genes |
nsv583585 |
Chr2:166170659 - 166216180 on Build GRCh38 |
Loss |
SCN9A
LOC101929680
|
nsv961905 |
Chr2:166198416 - 166199823 on Build GRCh38 |
Duplication |
SCN9A
LOC101929680
|
Product Details
- Assay Reference Genome
Location
Chr.2:166198514 on build GRCh38
- Cytoband
- 2q24.3
- Species
- Homo sapiens
- Variation Type
- Copy Number
Additional Information
For this assay, SNP(s) [rs111510277] 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
- 101929680
- Gene Symbol
- LOC101929680
- Gene Name
- uncharacterized LOC101929680
- Gene Aliases
- Location
- Chr.2:166081531-166301784 on build GRCh38
- Assay Gene Location
- Within Intron 3
- Entrez Gene ID
- 6335
- Gene Symbol
- SCN9A
- Gene Name
- sodium voltage-gated channel alpha subunit 9
- Gene Aliases
- ETHA, FEB3B, GEFSP7, HSAN2D, NE-NA, NENA, Nav1.7, PN1, SFNP
- Location
- Chr.2:166195185-166375987 on build GRCh38
- Assay Gene Location
- Within Exon 29
Target Copy Number Variation Details
- DGV Version
- Release date: 2016-05-15, GRCh GRCh38
Target Variation |
Location |
CNV Subtype |
Genes |
nsv583585 |
Chr2:166170659 - 166216180 on Build GRCh38 |
Loss |
SCN9A
LOC101929680
|
nsv961905 |
Chr2:166198416 - 166199823 on Build GRCh38 |
Duplication |
SCN9A
LOC101929680
|
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