Assay Details
Target Gene Details
Entrez Gene ID: | 9154 |
Gene Name: | solute carrier family 28 member 1 |
Gene Aliases: |
CNT1, HCNT1 |
Location: |
Chr.15:84884351-84975649 on Build GRCh38 |
Assay Gene Location: | Within Intron 6 |
Target Copy Number Variation Details
DGV Version: |
Release date: 2016-05-15, GRCh GRCh38 |
Target Variation |
Location | CNV Subtype |
Genes |
---|---|---|---|
nsv524050 | Chr.15:84864333 - 84935498 on Build GRCh38 | Loss | SLC28A1 ALPK3 |
nsv570289 | Chr.15:84887769 - 84905644 on Build GRCh38 | Loss | SLC28A1 |
nsv471257 | Chr.15:84869224 - 84919085 on Build GRCh38 | Gain | SLC28A1 ALPK3 |
esv3637099 | Chr.15:84858948 - 84903602 on Build GRCh38 | Gain | SLC28A1 ALPK3 |
esv2672879 | Chr.15:84183834 - 85188520 on Build GRCh38 | Deletion | GOLGA6L4 ZSCAN2 SCAND2P SLC28A1 LOC440300 NMB CSPG4P5 GOLGA6L5P SEC11A LINC00933 ZNF592 LOC102724135 LOC103171574 WDR73 UBE2Q2P1 UBE2Q2L LOC105376722 ALPK3 PDE8A GOLGA2P7 |
More Information
Additional Information:
For this assay, SNP(s) [rs75719247] 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 |