A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv3576659



Internal ID18874940
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr2:56311325..56488726hg38UCSC Ensembl
Innerchr2:56538460..56715861hg19UCSC Ensembl
Innerchr2:56391964..56569365hg18UCSC Ensembl
Cytoband2p16.1
Allele length
AssemblyAllele length
hg38177402
hg19177402
hg18177402
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv1004449
Supporting Variants
Samples
Known GenesCCDC85A
MethodSNP array
AnalysisAffymetrix SNP array copy number analysis
PlatformAffymetrix SNP Array 6.0
Comments
ReferenceCoe_et_al_2014
Pubmed ID25217958
Accession Number(s)nssv3576659
Frequency
Sample Size11257
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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