Assay Details
Target Gene Details
Entrez Gene ID: | 153129 |
Gene Name: | solute carrier family 38 member 9 |
Gene Aliases: |
URLC11 |
Location: |
Chr.5:55625845-55712344 on Build GRCh38 |
Assay Gene Location: | Within Exon 21 |
Target Copy Number Variation Details
DGV Version: |
Release date: 2016-05-15, GRCh GRCh38 |
Target Variation |
Location | CNV Subtype |
Genes |
---|---|---|---|
nsv830304 | Chr.5:55492810 - 55655813 on Build GRCh38 | Gain+Loss | SLC38A9 PLPP1 MIR5687 RNF138P1 |
nsv830305 | Chr.5:55543776 - 55743734 on Build GRCh38 | Loss | SLC38A9 DDX4 |
More Information
Additional Information:
For this assay, SNP(s) [rs75004233] 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 |