A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv16938895



Internal ID26651
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr3:142733088..142733238hg38UCSC Ensembl
chr3:142451930..142452080hg19UCSC Ensembl
Cytoband3q23
Allele length
AssemblyAllele length
hg38151
hg19151
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5445215
Supporting Variants
Samples
Known GenesTRPC1
MethodSequencing
Analysis
Platform
Comments
ReferenceByrska_Bishop_et_al_2022
Pubmed ID36055201
Accession Number(s)nssv16938895
Frequency
Sample Size3202
Observed Gain1
Observed Loss0
Observed Complex0
Frequency0.000156


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