A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv941225



Internal ID16235181
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr20:53858554..53859290hg38UCSC Ensembl
Innerchr20:52475093..52475829hg19UCSC Ensembl
Innerchr20:51908500..51909236hg18UCSC Ensembl
Cytoband20q13.2
Allele length
AssemblyAllele length
hg38737
hg19737
hg18737
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv586227
Supporting Variants
Samples
Known Genes
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nssv941225
Frequency
Sample Size17421
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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