A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv16937818



Internal ID25922
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr3:134293005..134296402hg38UCSC Ensembl
chr3:134011847..134015244hg19UCSC Ensembl
Cytoband3q22.2
Allele length
AssemblyAllele length
hg383398
hg193398
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5440424
Supporting Variants
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceByrska_Bishop_et_al_2022
Pubmed ID36055201
Accession Number(s)nssv16937818
Frequency
Sample Size3202
Observed Gain0
Observed Loss1
Observed Complex0
Frequency0.000312


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