A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5443282



Internal ID221682
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr3:8575980..8579556hg38UCSC Ensembl
chr3:8617666..8621242hg19UCSC Ensembl
Cytoband3p26.1
Allele length
AssemblyAllele length
hg383577
hg193577
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv16929796
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceByrska_Bishop_et_al_2022
Pubmed ID36055201
Accession Number(s)nsv5443282
Frequency
Sample Size3202
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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