A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv940723



Internal ID16234679
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr20:45575651..45577280hg38UCSC Ensembl
Innerchr20:44204290..44205919hg19UCSC Ensembl
Innerchr20:43637704..43639333hg18UCSC Ensembl
Cytoband20q13.12
Allele length
AssemblyAllele length
hg381630
hg191630
hg181630
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv586084
Supporting Variants
Samples
Known GenesWFDC8
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nssv940723
Frequency
Sample Size17421
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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