A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv937460



Internal ID16231416
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr20:5751309..5798259hg38UCSC Ensembl
Innerchr20:5731955..5778905hg19UCSC Ensembl
Innerchr20:5679955..5726905hg18UCSC Ensembl
Cytoband20p12.3
Allele length
AssemblyAllele length
hg3846951
hg1946951
hg1846951
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv585332
Supporting Variants
Samples
Known GenesC20orf196
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nssv937460
Frequency
Sample Size17421
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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