A curated catalogue of human genomic structural variation




Variant Details

Variant: dgv6158n223



Internal ID22809126
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr6:32638411..32761656hg38UCSC Ensembl
chr6:32606188..32729433hg19UCSC Ensembl
Cytoband6p21.32
Allele length
AssemblyAllele length
hg38123246
hg19123246
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnsv6406962, nsv6398487, nsv6398877, nsv6400084, nsv6409640, nsv6409225, nsv6397124
Samples
Known GenesHLA-DQA1, HLA-DQA2, HLA-DQB1, HLA-DQB2
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)dgv6158n223
Frequency
Sample Size19652
Observed Gain0
Observed Loss7
Observed Complex0
Frequencyn/a


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