A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv16980255



Internal ID54204
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr6:29943259..29944253hg38UCSC Ensembl
chr6:29911036..29912030hg19UCSC Ensembl
Cytoband6p22.1
Allele length
AssemblyAllele length
hg38995
hg19995
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5464278
Supporting Variants
Samples
Known GenesHLA-A
MethodSequencing
Analysis
Platform
Comments
ReferenceByrska_Bishop_et_al_2022
Pubmed ID36055201
Accession Number(s)nssv16980255
Frequency
Sample Size3202
Observed Gain0
Observed Loss1
Observed Complex0
Frequency0.14326


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