A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv1150986



Internal ID15877876
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr21:18685601..18717786hg38UCSC Ensembl
Innerchr21:20057919..20090104hg19UCSC Ensembl
Innerchr21:18979790..19011975hg18UCSC Ensembl
Cytoband21q21.1
Allele length
AssemblyAllele length
hg3832186
hg1932186
hg1832186
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv587149
Supporting Variants
SamplesHGDP01059
Known Genes
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nssv1150986
Frequency
Sample Size17421
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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