A curated catalogue of human genomic structural variation




Variant Details

Variant: dgv338n206



Internal ID22755642
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr3:4092357..4142769hg38UCSC Ensembl
chr3:4134041..4184453hg19UCSC Ensembl
Cytoband3p26.1
Allele length
AssemblyAllele length
hg3850413
hg1950413
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnsv5447372, nsv5438580
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceByrska_Bishop_et_al_2022
Pubmed ID36055201
Accession Number(s)dgv338n206
Frequency
Sample Size3202
Observed Gain0
Observed Loss2
Observed Complex0
Frequencyn/a


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