Assay Details
Target Gene Details
Entrez Gene ID: | 1006 |
Gene Name: | cadherin 8 |
Gene Aliases: |
Nbla04261 |
Location: |
Chr.16:61640435-62036835 on Build GRCh38 |
Assay Gene Location: | Within Exon 14 |
Gene Symbol | Transcript Accession | Exon Location | Assay Transcript Location | Protein ID |
---|---|---|---|---|
CDH8 | XM_005255760.3 | 13 | 7283 | XP_005255817.1 |
Target Copy Number Variation Details
DGV Version: |
Release date: 2016-05-15, GRCh GRCh38 |
Target Variation |
Location | CNV Subtype |
Genes |
---|---|---|---|
esv2661093 | Chr.16:61639003 - 61644336 on Build GRCh38 | Deletion | CDH8 |
esv3638781 | Chr.16:61638941 - 61644346 on Build GRCh38 | Loss | CDH8 |
nsv833256 | Chr.16:61558794 - 61736777 on Build GRCh38 | Gain | CDH8 |
nsv572844 | Chr.16:61625455 - 61690440 on Build GRCh38 | Loss | CDH8 |
esv2762088 | Chr.16:61220267 - 61799347 on Build GRCh38 | Gain+Loss | CDH8 |
More Information
Additional Information:
For this assay, SNP(s) [rs74344566] 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 |