A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv1156453



Internal ID15877644
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr9:20832096..20932869hg38UCSC Ensembl
Innerchr9:20832095..20932868hg19UCSC Ensembl
Innerchr9:20822095..20922868hg18UCSC Ensembl
Cytoband9p21.3
Allele length
AssemblyAllele length
hg38100774
hg19100774
hg18100774
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv613750
Supporting Variants
SamplesHGDP01021
Known GenesFOCAD
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nssv1156453
Frequency
Sample Size17421
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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