A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5483704



Internal ID261135
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr8:81204516..81213196hg38UCSC Ensembl
chr8:82116751..82125431hg19UCSC Ensembl
Cytoband8q21.13
Allele length
AssemblyAllele length
hg388681
hg198681
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17013896
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceByrska_Bishop_et_al_2022
Pubmed ID36055201
Accession Number(s)nsv5483704
Frequency
Sample Size3202
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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