A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv18142217



Internal ID20709257
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr6:32655651..32754355hg38UCSC Ensembl
chr6:32623428..32722132hg19UCSC Ensembl
Cytoband6p21.32
Allele length
AssemblyAllele length
hg3898705
hg1998705
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6406962
Supporting Variants
Samples
Known GenesHLA-DQA2, HLA-DQB1
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nssv18142217
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequency0.00017


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