A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv16937973



Internal ID26036
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr3:114110405..114110998hg38UCSC Ensembl
chr3:113829252..113829845hg19UCSC Ensembl
Cytoband3q13.31
Allele length
AssemblyAllele length
hg38594
hg19594
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5450022
Supporting Variants
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceByrska_Bishop_et_al_2022
Pubmed ID36055201
Accession Number(s)nssv16937973
Frequency
Sample Size3202
Observed Gain0
Observed Loss1
Observed Complex0
Frequency0.000312


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