Assay Details
Target Gene Details
Entrez Gene ID: | 57685 |
Gene Name: | cache domain containing 1 |
Gene Aliases: |
- |
Location: |
Chr.1:64470793-64693058 on Build GRCh38 |
Assay Gene Location: | Within Intron 1 |
| Gene Symbol | Transcript Accession | Exon Location | Assay Transcript Location | Protein ID |
|---|---|---|---|---|
| CACHD1 | NM_020925.2 | NP_065976.2 | ||
| CX163220.1 |
Target Copy Number Variation Details
DGV Version: |
Release date: 2016-05-15, GRCh GRCh38 |
| Target Variation |
Location | CNV Subtype |
Genes |
|---|---|---|---|
| nsv1122355 | Chr.1:64477933 - 64492378 on Build GRCh38 | Deletion |
|
| nsv546437 | Chr.1:64230394 - 64538095 on Build GRCh38 | Loss |
|
| esv2660804 | Chr.1:64381364 - 64626908 on Build GRCh38 | Deletion |
|
| esv3586265 | Chr.1:64420465 - 64489064 on Build GRCh38 | Loss |
|
| nsv830048 | Chr.1:64367523 - 64545238 on Build GRCh38 | Gain |
|
| nsv1000188 | Chr.1:64263100 - 64546875 on Build GRCh38 | Gain |
|
More Information
Additional Information:
For this assay, SNP(s) [rs115200638] 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: |
|

Genomic Map