A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv939291



Internal ID15886561
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr20:33656331..33663590hg38UCSC Ensembl
Innerchr20:32244137..32251396hg19UCSC Ensembl
Innerchr20:31707798..31715057hg18UCSC Ensembl
Cytoband20q11.22
Allele length
AssemblyAllele length
hg387260
hg197260
hg187260
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv585927
Supporting Variants
Samples
Known GenesC20orf144, NECAB3
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nssv939291
Frequency
Sample Size17421
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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