A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv602692



Internal ID16390101
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr6:32603062..32658342hg38UCSC Ensembl
Innerchr6:32570839..32626119hg19UCSC Ensembl
Innerchr6:32678817..32734097hg18UCSC Ensembl
Cytoband6p21.32
Allele length
AssemblyAllele length
hg3855281
hg1955281
hg1855281
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv1056405
Samples
Known GenesHLA-DQA1
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nsv602692
Frequency
Sample Size17421
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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