A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17009237



Internal ID73797
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr8:21408801..21415059hg38UCSC Ensembl
chr8:21266312..21272570hg19UCSC Ensembl
Cytoband8p21.3
Allele length
AssemblyAllele length
hg386259
hg196259
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5483933
Supporting Variants
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceByrska_Bishop_et_al_2022
Pubmed ID36055201
Accession Number(s)nssv17009237
Frequency
Sample Size3202
Observed Gain0
Observed Loss1
Observed Complex0
Frequency0.000312


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