A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv3116526



Internal ID21299792
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 StatusM
Merged Variantsdgv1023n145
Supporting Variantsnssv14089198, nssv14087595
Samplessample280, sample190
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)nsv3116526
Frequency
Sample Size467
Observed Gain0
Observed Loss2
Observed Complex0
Frequencyn/a


Hosted by The Centre for Applied Genomics
Grant support for DGV
Please read the usage disclaimer