A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv941601



Internal ID16235557
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr20:56832028..56851763hg38UCSC Ensembl
Innerchr20:55407084..55426819hg19UCSC Ensembl
Innerchr20:54840491..54860226hg18UCSC Ensembl
Cytoband20q13.31
Allele length
AssemblyAllele length
hg3819736
hg1919736
hg1819736
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv586307
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)nssv941601
Frequency
Sample Size17421
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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