Assay Details
Target Gene Details
Entrez Gene ID: | 388799 |
Gene Name: | family with sequence similarity 209 member B |
Gene Aliases: |
C20orf107, dJ1153D9.4 |
Location: |
Chr.20:56527124-56555626 on Build GRCh38 |
Assay Gene Location: |
Gene Symbol | Transcript Accession | Exon Location | Assay Transcript Location | Protein ID |
---|---|---|---|---|
FAM209B |
Target Copy Number Variation Details
DGV Version: |
Release date: 2016-05-15, GRCh GRCh38 |
Target Variation |
Location | CNV Subtype |
Genes |
---|---|---|---|
nsv525425 | Chr.20:56403979 - 56897294 on Build GRCh38 | Gain |
![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() |
nsv834015 | Chr.20:56518712 - 56656502 on Build GRCh38 | Loss |
![]() ![]() ![]() ![]() ![]() ![]() |
nsv1056574 | Chr.20:56495687 - 56761211 on Build GRCh38 | Gain |
![]() ![]() ![]() ![]() ![]() ![]() |
![](/order/genome-database/details/genotyping/assets/img/arrow_icon_up_black.png)
More Information
Additional Information:
For this assay, SNP(s) [rs74793016] 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: |
![]() ![]() ![]() |
![](/order/genome-database/details/genotyping/assets/img/arrow_icon_up_black.png)