Assay Details
Target Gene Details
Entrez Gene ID: | 57060 |
Gene Name: | poly(rC) binding protein 4 |
Gene Aliases: |
CBP, LIP4, MCG10 |
Location: |
Chr.3:51957454-51967466 on Build GRCh38 |
Assay Gene Location: | Within Intron 8 |
Target Copy Number Variation Details
DGV Version: |
Release date: 2016-05-15, GRCh GRCh38 |
Target Variation |
Location | CNV Subtype |
Genes |
---|---|---|---|
nsv1003453 | Chr.3:51928065 - 52065425 on Build GRCh38 | Gain | DUSP7 GPR62 PCBP4 LINC00696 ABHD14B PARP3 RPL29 ACY1 RRP9 ABHD14A-ACY1 ABHD14A |
nsv508922 | Chr.3:51940932 - 52009520 on Build GRCh38 | Insertion | GPR62 PCBP4 ABHD14B PARP3 RPL29 ACY1 RRP9 ABHD14A-ACY1 ABHD14A |
nsv954857 | Chr.3:51932485 - 52056584 on Build GRCh38 | Deletion | DUSP7 GPR62 PCBP4 ABHD14B PARP3 RPL29 ACY1 RRP9 ABHD14A-ACY1 ABHD14A |
nsv520211 | Chr.3:51738331 - 52132131 on Build GRCh38 | Gain | IQCF4 PCBP4 LINC00696 PARP3 ACY1 RRP9 ABHD14A-ACY1 IQCF3 ABHD14A DUSP7 IQCF1 IQCF6 GPR62 ABHD14B RPL29 IQCF5 POC1A IQCF2 IQCF5-AS1 |
More Information
Additional Information:
For this assay, SNP(s) [rs77484474] 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 |