A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv16937743



Internal ID25872
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr3:131351000..131408000hg38UCSC Ensembl
chr3:131069844..131126844hg19UCSC Ensembl
Cytoband3q22.1
Allele length
AssemblyAllele length
hg3857001
hg1957001
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5449190
Supporting Variants
Samples
Known GenesLOC339874, NUDT16, NUDT16P1
MethodSequencing
Analysis
Platform
Comments
ReferenceByrska_Bishop_et_al_2022
Pubmed ID36055201
Accession Number(s)nssv16937743
Frequency
Sample Size3202
Observed Gain1
Observed Loss0
Observed Complex0
Frequency0.000156


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