A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv1055697



Internal ID15908883
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr6:32549621..32572441hg38UCSC Ensembl
Innerchr6:32517398..32540218hg19UCSC Ensembl
Innerchr6:32625376..32648196hg18UCSC Ensembl
Cytoband6p21.32
Allele length
AssemblyAllele length
hg3822821
hg1922821
hg1822821
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv602493
Supporting Variants
Samples
Known GenesHLA-DRB6
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nssv1055697
Frequency
Sample Size17421
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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