A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv16929931



Internal ID20691
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr3:3883097..4073514hg38UCSC Ensembl
chr3:3924781..4115198hg19UCSC Ensembl
Cytoband3p26.1
Allele length
AssemblyAllele length
hg38190418
hg19190418
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5437922
Supporting Variants
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceByrska_Bishop_et_al_2022
Pubmed ID36055201
Accession Number(s)nssv16929931
Frequency
Sample Size3202
Observed Gain0
Observed Loss1
Observed Complex0
Frequency0.000312


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