A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv940962



Internal ID15888232
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr20:46340501..46387008hg38UCSC Ensembl
Innerchr20:44969139..45015647hg19UCSC Ensembl
Innerchr20:44402546..44449054hg18UCSC Ensembl
Cytoband20q13.12
Allele length
AssemblyAllele length
hg3846508
hg1946509
hg1846509
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv586155
Supporting Variants
Samples
Known GenesELMO2, SLC35C2
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nssv940962
Frequency
Sample Size17421
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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