A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv939222



Internal ID16233178
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr20:31216378..31257056hg38UCSC Ensembl
Innerchr20:29804208..29844859hg19UCSC Ensembl
Innerchr20:29267869..29308520hg18UCSC Ensembl
Cytoband20q11.21
Allele length
AssemblyAllele length
hg3840679
hg1940652
hg1840652
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv585888
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)nssv939222
Frequency
Sample Size17421
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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