Assay Details
Target Gene Details
Entrez Gene ID: | 64111 |
Gene Name: | neuropeptide VF precursor |
Gene Aliases: |
C7orf9, RFRP |
Location: |
Chr.7:25224570-25228486 on Build GRCh38 |
Assay Gene Location: | Within Exon 3 |
Gene Symbol | Transcript Accession | Exon Location | Assay Transcript Location | Protein ID |
---|---|---|---|---|
NPVF | NM_022150.3 | 3 | 945 | NP_071433.3 |
AF440392.1 | 3 | 945 | AAL90453.1 |
Target Copy Number Variation Details
DGV Version: |
Release date: 2016-05-15, GRCh GRCh38 |
Target Variation |
Location | CNV Subtype |
Genes |
---|---|---|---|
nsv606424 | Chr.7:24942910 - 25426902 on Build GRCh38 | Gain | OSBPL3 C7orf31 CYCS NPVF |
nsv522075 | Chr.7:25224281 - 25224937 on Build GRCh38 | Loss | NPVF |
nsv606426 | Chr.7:25214506 - 25581959 on Build GRCh38 | Gain | NPVF |
More Information
Additional Information:
For this assay, SNP(s) [rs146193251] 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.
Set Membership: |
Intragenic Exonic DGV Variation |