A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv3116052



Internal ID21299318
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr6:32444783..32551793hg38UCSC Ensembl
Innerchr6:32412560..32519570hg19UCSC Ensembl
Cytoband6p21.32
Allele length
AssemblyAllele length
hg38107011
hg19107011
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv1022n145
Supporting Variantsnssv14086412, nssv14083742
Samplessample71, sample140
Known GenesHLA-DRA, HLA-DRB5
MethodOligo aCGH
Analysis
Platform
Comments
ReferenceLu_et_al_2017
Pubmed ID28705883
Accession Number(s)nsv3116052
Frequency
Sample Size467
Observed Gain0
Observed Loss2
Observed Complex0
Frequencyn/a


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