A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv585930



Internal ID16026653
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr20:33779897..33839036hg38UCSC Ensembl
Innerchr20:32367703..32426842hg19UCSC Ensembl
Innerchr20:31831364..31890503hg18UCSC Ensembl
Cytoband20q11.22
Allele length
AssemblyAllele length
hg3859140
hg1959140
hg1859140
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv1152385
SamplesHGDP01364
Known GenesCHMP4B, ZNF341
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nsv585930
Frequency
Sample Size17421
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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