Assay Details
Target Gene Details
Entrez Gene ID: | 105379393 |
Gene Name: | uncharacterized LOC105379393 |
Gene Aliases: |
- |
Location: |
Chr.8:42051750-42104987 on Build GRCh38 |
Assay Gene Location: | Within Intron 1 |
Gene Symbol | Transcript Accession | Exon Location | Assay Transcript Location | Protein ID |
---|---|---|---|---|
LOC105379393 | NR_136589.1 | |||
HY030269.1 |
Target Copy Number Variation Details
DGV Version: |
Release date: 2016-05-15, GRCh GRCh38 |
Target Variation |
Location | CNV Subtype |
Genes |
---|---|---|---|
nsv6168 | Chr.8:42092972 - 42137630 on Build GRCh38 | Deletion | LOC105379393 |
nsv1022636 | Chr.8:42093555 - 42134046 on Build GRCh38 | Loss | LOC105379393 |
More Information
Additional Information:
For this assay, SNP(s) [rs150947192] 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 Intronic Non-exonic DGV Variation |