A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv940869



Internal ID15888139
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr20:45727555..45778454hg38UCSC Ensembl
Innerchr20:44356194..44407093hg19UCSC Ensembl
Innerchr20:43789608..43840500hg18UCSC Ensembl
Cytoband20q13.12
Allele length
AssemblyAllele length
hg3850900
hg1950900
hg1850893
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv586131
Supporting Variants
Samples
Known GenesWFDC3
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nssv940869
Frequency
Sample Size17421
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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