A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5443359



Internal ID221760
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr3:145677285..145679926hg38UCSC Ensembl
chr3:145395072..145397713hg19UCSC Ensembl
Cytoband3q24
Allele length
AssemblyAllele length
hg382642
hg192642
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv16938934
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceByrska_Bishop_et_al_2022
Pubmed ID36055201
Accession Number(s)nsv5443359
Frequency
Sample Size3202
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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