A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv581507



Internal ID16368916
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr2:40595886..40669245hg38UCSC Ensembl
Innerchr2:40823026..40896385hg19UCSC Ensembl
Innerchr2:40676530..40749889hg18UCSC Ensembl
Cytoband2p22.1
Allele length
AssemblyAllele length
hg3873360
hg1973360
hg1873360
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv6797n54
Supporting Variantsnssv1151046
SamplesHGDP00710
Known Genes
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nsv581507
Frequency
Sample Size17421
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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