Assay Details
Target Gene Details
Entrez Gene ID: | 387804 |
Gene Name: | V-set and transmembrane domain containing 5 |
Gene Aliases: |
C11orf90 |
Location: |
Chr.11:93817315-93850653 on Build GRCh38 |
Assay Gene Location: | Within Intron 1 |
Gene Symbol | Transcript Accession | Exon Location | Assay Transcript Location | Protein ID |
---|---|---|---|---|
VSTM5 | NM_001144871.1 | NP_001138343.1 | ||
DY654877.1 |
Target Copy Number Variation Details
DGV Version: |
Release date: 2016-05-15, GRCh GRCh38 |
Target Variation |
Location | CNV Subtype |
Genes |
---|---|---|---|
esv3892068 | Chr.11:93819689 - 93897325 on Build GRCh38 | Gain | VSTM5 |
esv3627294 | Chr.11:93485306 - 93944317 on Build GRCh38 | Gain | SNORD6 C11orf54 MIR1304 CEP295 VSTM5 TAF1D SMCO4 SNORA18 SNORA1 SNORA8 SNORA40 SCARNA9 MED17 SNORD5 SNORA32 SNORA25 |
More Information
Additional Information:
For this assay, SNP(s) [rs76747239] 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 |