A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv16936818



Internal ID25265
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr3:98742979..98743273hg38UCSC Ensembl
chr3:98461823..98462117hg19UCSC Ensembl
Cytoband3q12.1
Allele length
AssemblyAllele length
hg38295
hg19295
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5435676
Supporting Variants
Samples
Known GenesST3GAL6
MethodSequencing
Analysis
Platform
Comments
ReferenceByrska_Bishop_et_al_2022
Pubmed ID36055201
Accession Number(s)nssv16936818
Frequency
Sample Size3202
Observed Gain0
Observed Loss1
Observed Complex0
Frequency0.000312


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