A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv16938659



Internal ID26505
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr3:116949807..116965810hg38UCSC Ensembl
chr3:116668654..116684657hg19UCSC Ensembl
Cytoband3q13.31
Allele length
AssemblyAllele length
hg3816004
hg1916004
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5449083
Supporting Variants
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceByrska_Bishop_et_al_2022
Pubmed ID36055201
Accession Number(s)nssv16938659
Frequency
Sample Size3202
Observed Gain0
Observed Loss1
Observed Complex0
Frequency0.000312


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