A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv16936972



Internal ID25361
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr3:94083487..94086604hg38UCSC Ensembl
chr3:93802331..93805448hg19UCSC Ensembl
Cytoband3q11.1
Allele length
AssemblyAllele length
hg383118
hg193118
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5442929
Supporting Variants
Samples
Known GenesNSUN3
MethodSequencing
Analysis
Platform
Comments
ReferenceByrska_Bishop_et_al_2022
Pubmed ID36055201
Accession Number(s)nssv16936972
Frequency
Sample Size3202
Observed Gain0
Observed Loss1
Observed Complex0
Frequency0.000312


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