A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv16937753



Internal ID25879
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr3:133384323..133384384hg38UCSC Ensembl
chr3:133103167..133103228hg19UCSC Ensembl
Cytoband3q22.1
Allele length
AssemblyAllele length
hg3862
hg1962
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5445462
Supporting Variants
Samples
Known GenesTMEM108
MethodSequencing
Analysis
Platform
Comments
ReferenceByrska_Bishop_et_al_2022
Pubmed ID36055201
Accession Number(s)nssv16937753
Frequency
Sample Size3202
Observed Gain1
Observed Loss0
Observed Complex0
Frequency0.136728


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