A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv582061



Internal ID16369470
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr2:56832996..57170288hg38UCSC Ensembl
Innerchr2:57060131..57397423hg19UCSC Ensembl
Innerchr2:56913635..57250927hg18UCSC Ensembl
Cytoband2p16.1
Allele length
AssemblyAllele length
hg38337293
hg19337293
hg18337293
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv1150454
SamplesHGDP00645
Known Genes
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nsv582061
Frequency
Sample Size17421
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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