Assay Details
Target Gene Details
Entrez Gene ID: | 29080 |
Gene Name: | coiled-coil domain containing 59 |
Gene Aliases: |
BR22, HSPC128, TAP26 |
Location: |
Chr.12:82352304-82358805 on Build GRCh38 |
Assay Gene Location: | Overlaps - Exon 5 |
Gene Symbol | Transcript Accession | Exon Location | Assay Transcript Location | Protein ID |
---|---|---|---|---|
CCDC59 | NM_014167.4 | NP_054886.2 | ||
NR_033192.1 |
Target Copy Number Variation Details
DGV Version: |
Release date: 2016-05-15, GRCh GRCh38 |
Target Variation |
Location | CNV Subtype |
Genes |
---|---|---|---|
nsv559539 | Chr.12:81887018 - 82502439 on Build GRCh38 | Gain |
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nsv832471 | Chr.12:82185174 - 82361581 on Build GRCh38 | Loss |
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nsv559541 | Chr.12:82321431 - 82714616 on Build GRCh38 | Gain |
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More Information
Additional Information:
For this assay, SNP(s) [rs114042587] 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: |
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Gene Ontology Categories:
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