A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5434928



Internal ID213589
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr3:145502164..145538253hg38UCSC Ensembl
chr3:145219951..145256040hg19UCSC Ensembl
Cytoband3q24
Allele length
AssemblyAllele length
hg3836090
hg1936090
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv16940748
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceByrska_Bishop_et_al_2022
Pubmed ID36055201
Accession Number(s)nsv5434928
Frequency
Sample Size3202
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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