A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv586113



Internal ID16373522
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr20:45576132..45579865hg38UCSC Ensembl
Innerchr20:44204771..44208504hg19UCSC Ensembl
Innerchr20:43638185..43641918hg18UCSC Ensembl
Cytoband20q13.12
Allele length
AssemblyAllele length
hg383734
hg193734
hg183734
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv940834
Samples
Known GenesWFDC8
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nsv586113
Frequency
Sample Size17421
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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