A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv1056633



Internal ID15909819
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr6:32642819..32656837hg38UCSC Ensembl
Innerchr6:32610596..32624614hg19UCSC Ensembl
Innerchr6:32718574..32732592hg18UCSC Ensembl
Cytoband6p21.32
Allele length
AssemblyAllele length
hg3814019
hg1914019
hg1814019
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv602745
Supporting Variants
Samples
Known GenesHLA-DQA1
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nssv1056633
Frequency
Sample Size17421
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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