A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv603585



Internal ID16390994
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr6:66994928..67267433hg38UCSC Ensembl
Innerchr6:67704821..67977326hg19UCSC Ensembl
Innerchr6:67761542..68034047hg18UCSC Ensembl
Cytoband6q12
Allele length
AssemblyAllele length
hg38272506
hg19272506
hg18272506
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv1154799
SamplesHGDP00185
Known Genes
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nsv603585
Frequency
Sample Size17421
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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