A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv1055695



Internal ID15908881
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr6:32543895..32663681hg38UCSC Ensembl
Innerchr6:32511672..32631458hg19UCSC Ensembl
Innerchr6:32619650..32739436hg18UCSC Ensembl
Cytoband6p21.32
Allele length
AssemblyAllele length
hg38119787
hg19119787
hg18119787
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv602491
Supporting Variants
Samples
Known GenesHLA-DQA1, HLA-DQB1, HLA-DRB1, HLA-DRB6
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nssv1055695
Frequency
Sample Size17421
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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