A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5441716



Internal ID220173
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr3:48488505..48497513hg38UCSC Ensembl
Cytoband
Allele length
AssemblyAllele length
hg389009
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv16933732
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceByrska_Bishop_et_al_2022
Pubmed ID36055201
Accession Number(s)nsv5441716
Frequency
Sample Size3202
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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