A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5448566



Internal ID226837
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr3:139424494..139433390hg38UCSC Ensembl
chr3:139143336..139152232hg19UCSC Ensembl
Cytoband3q23
Allele length
AssemblyAllele length
hg388897
hg198897
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv16938798
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceByrska_Bishop_et_al_2022
Pubmed ID36055201
Accession Number(s)nsv5448566
Frequency
Sample Size3202
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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