A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv16930498



Internal ID21077
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr3:16611176..16617234hg38UCSC Ensembl
chr3:16652683..16658741hg19UCSC Ensembl
Cytoband3p24.3
Allele length
AssemblyAllele length
hg386059
hg196059
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5443052
Supporting Variants
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceByrska_Bishop_et_al_2022
Pubmed ID36055201
Accession Number(s)nssv16930498
Frequency
Sample Size3202
Observed Gain0
Observed Loss1
Observed Complex0
Frequency0.004531


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