A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv938912



Internal ID16232868
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr20:21926142..21987312hg38UCSC Ensembl
Innerchr20:21906780..21967950hg19UCSC Ensembl
Innerchr20:21854780..21915950hg18UCSC Ensembl
Cytoband20p11.22
Allele length
AssemblyAllele length
hg3861171
hg1961171
hg1861171
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv585716
Supporting Variants
Samples
Known Genes
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nssv938912
Frequency
Sample Size17421
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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