A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv16931852



Internal ID21965
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr3:38113464..38113584hg38UCSC Ensembl
chr3:38154955..38155075hg19UCSC Ensembl
Cytoband3p22.2
Allele length
AssemblyAllele length
hg38121
hg19121
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5442653
Supporting Variants
Samples
Known GenesDLEC1
MethodSequencing
Analysis
Platform
Comments
ReferenceByrska_Bishop_et_al_2022
Pubmed ID36055201
Accession Number(s)nssv16931852
Frequency
Sample Size3202
Observed Gain0
Observed Loss1
Observed Complex0
Frequency0.165938


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