A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv936074



Internal ID16230030
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr20:1580578..1611843hg38UCSC Ensembl
Innerchr20:1561224..1592489hg19UCSC Ensembl
Innerchr20:1509224..1540489hg18UCSC Ensembl
Cytoband20p13
Allele length
AssemblyAllele length
hg3831266
hg1931266
hg1831266
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv585241
Supporting Variants
Samples
Known GenesSIRPB1
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nssv936074
Frequency
Sample Size17421
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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