A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv3117635



Internal ID21300901
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr6:32444783..32664198hg38UCSC Ensembl
Innerchr6:32412560..32631975hg19UCSC Ensembl
Cytoband6p21.32
Allele length
AssemblyAllele length
hg38219416
hg19219416
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv1023n145
Supporting Variantsnssv14082946, nssv14083782
Samplessample83, sample321
Known GenesHLA-DQA1, HLA-DQB1, HLA-DRA, HLA-DRB1, HLA-DRB5, HLA-DRB6
MethodOligo aCGH
Analysis
Platform
Comments
ReferenceLu_et_al_2017
Pubmed ID28705883
Accession Number(s)nsv3117635
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