A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv14087595



Internal ID21273396
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr6:32444783..32641069hg38UCSC Ensembl
Innerchr6:32412560..32608846hg19UCSC Ensembl
Cytoband6p21.32
Allele length
AssemblyAllele length
hg38196287
hg19196287
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv3116526
Supporting Variants
Samplessample190
Known GenesHLA-DQA1, HLA-DRA, HLA-DRB1, HLA-DRB5, HLA-DRB6
MethodOligo aCGH
Analysis
Platform
Comments
ReferenceLu_et_al_2017
Pubmed ID28705883
Accession Number(s)nssv14087595
Frequency
Sample Size467
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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