A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv590140



Internal ID16030863
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr3:41859164..42025885hg38UCSC Ensembl
Innerchr3:41900656..42067377hg19UCSC Ensembl
Innerchr3:41875660..42042381hg18UCSC Ensembl
Cytoband3p22.1
Allele length
AssemblyAllele length
hg38166722
hg19166722
hg18166722
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv8296n54
Supporting Variantsnssv1151765
SamplesHGDP00905
Known GenesULK4
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nsv590140
Frequency
Sample Size17421
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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