A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5483358



Internal ID260795
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr8:11878997..11881417hg38UCSC Ensembl
chr8:11736506..11738926hg19UCSC Ensembl
Cytoband8p23.1
Allele length
AssemblyAllele length
hg382421
hg192421
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17008738
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceByrska_Bishop_et_al_2022
Pubmed ID36055201
Accession Number(s)nsv5483358
Frequency
Sample Size3202
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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