Assay Details
Target Gene Details
Entrez Gene ID: | 105371932 |
Gene Name: | uncharacterized LOC105371932 |
Gene Aliases: |
- |
Location: |
Chr.17:35240043-35247472 on Build GRCh38 |
Assay Gene Location: | Within Intron 3 |
Gene Symbol | Transcript Accession | Exon Location | Assay Transcript Location | Protein ID |
---|---|---|---|---|
LOC105371932 | XM_017025492.1 | XP_016880981.1 |
Target Copy Number Variation Details
DGV Version: |
Release date: 2016-05-15, GRCh GRCh38 |
Target Variation |
Location | CNV Subtype |
Genes |
---|---|---|---|
esv2422399 | Chr.17:35212221 - 35291582 on Build GRCh38 | Deletion | SLFN5 LOC105371932 |
esv3892998 | Chr.17:35106468 - 35295755 on Build GRCh38 | Loss | FNDC8 UNC45B SLC35G3 NLE1 RAD51D RAD51L3-RFFL SLFN5 LOC105371932 |
nsv574741 | Chr.17:35225256 - 35500115 on Build GRCh38 | Loss | SLFN12L SLFN11 SLFN5 LOC105371933 LOC105371932 SLFN12 SLFN13 |
More Information
Additional Information:
For this assay, SNP(s) [rs114664206] 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 |