A curated catalogue of human genomic structural variation




Variant Details

Variant: dgv1023n145



Internal ID22814039
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr6:32444783..32666862hg38UCSC Ensembl
chr6:32412560..32634639hg19UCSC Ensembl
Cytoband6p21.32
Allele length
AssemblyAllele length
hg38222080
hg19222080
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnsv3116789, nsv3118275, nsv3110352, nsv3111540, nsv3116526, nsv3117635
Samplessample83, sample382, sample280, sample80, sample156, sample256, sample190, sample95, sample29, sample216, sample231, sample61, sample6, sample43, sample175, sample245, sample117, sample278, sample335, sample321, sample163
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)dgv1023n145
Frequency
Sample Size467
Observed Gain0
Observed Loss21
Observed Complex0
Frequencyn/a


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