A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6012493



Internal ID21921836
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr6:32687969..32776099hg38UCSC Ensembl
chr6:32655746..32743876hg19UCSC Ensembl
Cytoband6p21.32
Allele length
AssemblyAllele length
hg3888131
hg1988131
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17567310
Samples
Known GenesHLA-DQA2, HLA-DQB2
MethodSequencing
Analysis
Platform
Comments
ReferenceWu_et_al_2021
Pubmed ID34764282
Accession Number(s)nsv6012493
Frequency
Sample Size405
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


Hosted by The Centre for Applied Genomics
Grant support for DGV
Please read the usage disclaimer