A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv16945928



Internal ID31293
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr3:192935287..192968491hg38UCSC Ensembl
chr3:192653076..192686280hg19UCSC Ensembl
Cytoband3q29
Allele length
AssemblyAllele length
hg3833205
hg1933205
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5445087
Supporting Variants
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceByrska_Bishop_et_al_2022
Pubmed ID36055201
Accession Number(s)nssv16945928
Frequency
Sample Size3202
Observed Gain0
Observed Loss1
Observed Complex0
Frequency0.000312


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