A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv16938894



Internal ID26650
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr3:142727909..142727976hg38UCSC Ensembl
chr3:142446751..142446818hg19UCSC Ensembl
Cytoband3q23
Allele length
AssemblyAllele length
hg3868
hg1968
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5449727
Supporting Variants
Samples
Known GenesTRPC1
MethodSequencing
Analysis
Platform
Comments
ReferenceByrska_Bishop_et_al_2022
Pubmed ID36055201
Accession Number(s)nssv16938894
Frequency
Sample Size3202
Observed Gain0
Observed Loss1
Observed Complex0
Frequency0.000312


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