A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv938917



Internal ID16232873
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr20:23444001..23588763hg38UCSC Ensembl
Innerchr20:23424638..23569400hg19UCSC Ensembl
Innerchr20:23372638..23517400hg18UCSC Ensembl
Cytoband20p11.21
Allele length
AssemblyAllele length
hg38144763
hg19144763
hg18144763
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv585722
Supporting Variants
Samples
Known GenesCST11, CST13P, CST8, CST9L, CSTL1
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nssv938917
Frequency
Sample Size17421
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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