A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv1056621



Internal ID15909807
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr6:32642282..32643864hg38UCSC Ensembl
Innerchr6:32610059..32611641hg19UCSC Ensembl
Innerchr6:32718037..32719619hg18UCSC Ensembl
Cytoband6p21.32
Allele length
AssemblyAllele length
hg381583
hg191583
hg181583
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv602738
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)nssv1056621
Frequency
Sample Size17421
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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