A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv3116789



Internal ID21300055
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr6:32444783..32613714hg38UCSC Ensembl
Innerchr6:32412560..32581491hg19UCSC Ensembl
Cytoband6p21.32
Allele length
AssemblyAllele length
hg38168932
hg19168932
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv1023n145
Supporting Variantsnssv14086296, nssv14087853, nssv14086533, nssv14086498
Samplessample156, sample256, sample117, sample163
Known GenesHLA-DRA, HLA-DRB1, HLA-DRB5, HLA-DRB6
MethodOligo aCGH
Analysis
Platform
Comments
ReferenceLu_et_al_2017
Pubmed ID28705883
Accession Number(s)nsv3116789
Frequency
Sample Size467
Observed Gain0
Observed Loss4
Observed Complex0
Frequencyn/a


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