A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv16929314



Internal ID20263
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr3:4198457..4240464hg38UCSC Ensembl
chr3:4240141..4282148hg19UCSC Ensembl
Cytoband3p26.1
Allele length
AssemblyAllele length
hg3842008
hg1942008
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5446626
Supporting Variants
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceByrska_Bishop_et_al_2022
Pubmed ID36055201
Accession Number(s)nssv16929314
Frequency
Sample Size3202
Observed Gain0
Observed Loss1
Observed Complex0
Frequency0.000781


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