Assay Details
Target Gene Details
Entrez Gene ID: | 105373878 |
Gene Name: | uncharacterized LOC105373878 |
Gene Aliases: |
- |
Location: |
Chr.2:217978707-217992615 on Build GRCh38 |
Assay Gene Location: | Overlaps Intron 3 - Exon 4 |
Gene Symbol | Transcript Accession | Exon Location | Assay Transcript Location | Protein ID |
---|---|---|---|---|
LOC105373878 | NR_135524.1 | |||
DB245334.1 |
Target Copy Number Variation Details
DGV Version: |
Release date: 2016-05-15, GRCh GRCh38 |
Target Variation |
Location | CNV Subtype |
Genes |
---|---|---|---|
nsv834541 | Chr.2:217838312 - 218052028 on Build GRCh38 | Loss | RUFY4 LOC105373879 LOC105373878 TNS1 MIR6809 |
More Information
Additional Information:
For this assay, SNP(s) [rs74411550] 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 Non-exonic DGV Variation |