A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv18142223



Internal ID20709263
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr6:32662527..32759405hg38UCSC Ensembl
chr6:32630304..32727182hg19UCSC Ensembl
Cytoband6p21.32
Allele length
AssemblyAllele length
hg3896879
hg1996879
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6409640
Supporting Variants
Samples
Known GenesHLA-DQA2, HLA-DQB1, HLA-DQB2
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nssv18142223
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequency0.09014


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