A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv3559370



Internal ID18857651
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr16:62155698..62251211hg38UCSC Ensembl
Innerchr16:62189602..62285115hg19UCSC Ensembl
Innerchr16:60747103..60842616hg18UCSC Ensembl
Cytoband16q21
Allele length
AssemblyAllele length
hg3895514
hg1995514
hg1895514
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv1066411
Supporting Variants
Samples
Known Genes
MethodSNP array
AnalysisAffymetrix SNP array copy number analysis
PlatformAffymetrix SNP Array 6.0
Comments
ReferenceCoe_et_al_2014
Pubmed ID25217958
Accession Number(s)nssv3559370
Frequency
Sample Size11257
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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