A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv16929284



Internal ID20236
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr3:4073830..4120314hg38UCSC Ensembl
chr3:4115514..4161998hg19UCSC Ensembl
Cytoband3p26.1
Allele length
AssemblyAllele length
hg3846485
hg1946485
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5449365
Supporting Variants
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceByrska_Bishop_et_al_2022
Pubmed ID36055201
Accession Number(s)nssv16929284
Frequency
Sample Size3202
Observed Gain0
Observed Loss1
Observed Complex0
Frequency0.001562


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