A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5443599



Internal ID221993
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr3:107406264..107406497hg38UCSC Ensembl
chr3:107125111..107125344hg19UCSC Ensembl
Cytoband3q13.12
Allele length
AssemblyAllele length
hg38234
hg19234
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv16937895
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceByrska_Bishop_et_al_2022
Pubmed ID36055201
Accession Number(s)nsv5443599
Frequency
Sample Size3202
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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