A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6006399



Internal ID21915742
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr6:32652351..32751554hg38UCSC Ensembl
chr6:32620128..32719331hg19UCSC Ensembl
Cytoband6p21.32
Allele length
AssemblyAllele length
hg3899204
hg1999204
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17561315
Samples
Known GenesHLA-DQA2, HLA-DQB1
MethodSequencing
Analysis
Platform
Comments
ReferenceWu_et_al_2021
Pubmed ID34764282
Accession Number(s)nsv6006399
Frequency
Sample Size405
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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