A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv3576656



Internal ID18528251
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr2:55146426..55223008hg38UCSC Ensembl
Innerchr2:55373562..55450144hg19UCSC Ensembl
Innerchr2:55227066..55303648hg18UCSC Ensembl
Cytoband2p16.1
Allele length
AssemblyAllele length
hg3876583
hg1976583
hg1876583
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv1010438
Supporting Variants
Samples
Known GenesCLHC1
MethodSNP array
AnalysisAffymetrix SNP array copy number analysis
PlatformAffymetrix SNP Array 6.0
Comments
ReferenceCoe_et_al_2014
Pubmed ID25217958
Accession Number(s)nssv3576656
Frequency
Sample Size29084
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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