A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv1150956



Internal ID15532962
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr20:47828020..48524983hg38UCSC Ensembl
Innerchr20:46456764..47141521hg19UCSC Ensembl
Innerchr20:45890171..46574928hg18UCSC Ensembl
Cytoband20q13.13
Allele length
AssemblyAllele length
hg38696964
hg19684758
hg18684758
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv586157
Supporting Variants
SamplesHGDP01412
Known GenesLINC00494
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nssv1150956
Frequency
Sample Size17421
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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