Assay Details
Target Gene Details
Entrez Gene ID: | 220965 |
Gene Name: | family with sequence similarity 13 member C |
Gene Aliases: |
FAM13C1 |
Location: |
Chr.10:59245933-59363186 on Build GRCh38 |
Assay Gene Location: | Within Intron 16 |
Target Copy Number Variation Details
DGV Version: |
Release date: 2016-05-15, GRCh GRCh38 |
Target Variation |
Location | CNV Subtype |
Genes |
---|---|---|---|
nsv831888 | Chr.10:59183895 - 59378493 on Build GRCh38 | Gain | PHYHIPL FAM13C |
More Information
Additional Information:
For this assay, SNP(s) [rs148429451] 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 |