Target Copy Number Variation Details
- DGV Version
- Release date: 2016-05-15, GRCh GRCh38
Target
Variation ID |
Location |
CNV
Subtype |
Genes |
| nsv831873 |
Chr10:50950850 - 51139780 on Build GRCh38 |
Gain |
 LOC102724719
PRKG1
|
| nsv831872 |
Chr10:50903568 - 51058777 on Build GRCh38 |
Gain |
PRKG1
|
Product Details
- Assay Reference Genome
Location
Chr.10:51001806 on build GRCh38- Cytoband
- 10q11.23
- Species
- Homo sapiens
- Variation Type
- Copy Number
Additional Information
For this assay, SNP(s) [rs79626168] 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
- 5592
- Gene Symbol
- PRKG1
- Gene Name
- protein kinase, cGMP-dependent, type I
- Gene Aliases
- AAT8, PKG, PRKG1B, PRKGR1B, cGK, cGK 1, cGK1, cGKI, cGKI-BETA, cGKI-alpha
- Location
- Chr.10:50991151-52298350 on build GRCh38
- Assay Gene Location
- Within Intron 1
Target Copy Number Variation Details
- DGV Version
- Release date: 2016-05-15, GRCh GRCh38
Target
Variation |
Location |
CNV
Subtype |
Genes |
| nsv831873 |
Chr10:50950850 - 51139780 on Build GRCh38 |
Gain |
LOC102724719
PRKG1
|
| nsv831872 |
Chr10:50903568 - 51058777 on Build GRCh38 |
Gain |
PRKG1
|
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