A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv3559842



Internal ID18858123
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr16:82059578..82126262hg38UCSC Ensembl
Innerchr16:82093183..82159867hg19UCSC Ensembl
Innerchr16:80650684..80717368hg18UCSC Ensembl
Cytoband16q23.3
Allele length
AssemblyAllele length
hg3866685
hg1966685
hg1866685
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv1061709
Supporting Variants
Samples
Known GenesHSD17B2
MethodSNP array
AnalysisAffymetrix SNP array copy number analysis
PlatformAffymetrix SNP Array 6.0
Comments
ReferenceCoe_et_al_2014
Pubmed ID25217958
Accession Number(s)nssv3559842
Frequency
Sample Size11257
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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