A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv16940348



Internal ID27613
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr3:141272528..141272705hg38UCSC Ensembl
chr3:140991370..140991547hg19UCSC Ensembl
Cytoband3q23
Allele length
AssemblyAllele length
hg38178
hg19178
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5446555
Supporting Variants
Samples
Known GenesACPL2
MethodSequencing
Analysis
Platform
Comments
ReferenceByrska_Bishop_et_al_2022
Pubmed ID36055201
Accession Number(s)nssv16940348
Frequency
Sample Size3202
Observed Gain1
Observed Loss0
Observed Complex0
Frequency0.121293


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