A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv16934111



Internal ID23472
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr3:73013518..73026685hg38UCSC Ensembl
chr3:73062669..73075836hg19UCSC Ensembl
Cytoband3p13
Allele length
AssemblyAllele length
hg3813168
hg1913168
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5440176
Supporting Variants
Samples
Known GenesPPP4R2
MethodSequencing
Analysis
Platform
Comments
ReferenceByrska_Bishop_et_al_2022
Pubmed ID36055201
Accession Number(s)nssv16934111
Frequency
Sample Size3202
Observed Gain0
Observed Loss1
Observed Complex0
Frequency0.000312


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