Target Copy Number Variation Details
- DGV Version
- Release date: 2016-05-15, GRCh GRCh38
Target Variation ID |
Location |
CNV Subtype |
Genes |
nsv1521 |
Chr1:7954179 - 7987433 on Build GRCh38 |
Insertion |
PARK7
|
Product Details
- Assay Reference Genome
Location
Chr.1:7969520 on build GRCh38
- Cytoband
- 1p36.23
- Species
- Homo sapiens
- Variation Type
- Copy Number
Additional Information
For this assay, SNP(s) [rs141737779] 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
- 11315
- Gene Symbol
- PARK7
- Gene Name
- Parkinsonism associated deglycase
- Gene Aliases
- DJ-1, DJ1, HEL-S-67p
- Location
- Chr.1:7961654-7985282 on build GRCh38
- Assay Gene Location
- Within Intron 5
Target Copy Number Variation Details
- DGV Version
- Release date: 2016-05-15, GRCh GRCh38
Target Variation |
Location |
CNV Subtype |
Genes |
nsv1521 |
Chr1:7954179 - 7987433 on Build GRCh38 |
Insertion |
PARK7
|
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