A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv1056636



Internal ID15909822
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr6:32642819..32658394hg38UCSC Ensembl
Innerchr6:32610596..32626171hg19UCSC Ensembl
Innerchr6:32718574..32734149hg18UCSC Ensembl
Cytoband6p21.32
Allele length
AssemblyAllele length
hg3815576
hg1915576
hg1815576
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv602747
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)nssv1056636
Frequency
Sample Size17421
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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