A curated catalogue of human genomic structural variation




Variant Details

Variant: dgv339n206



Internal ID22755643
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr3:4110265..4271913hg38UCSC Ensembl
chr3:4151949..4313597hg19UCSC Ensembl
Cytoband3p26.1
Allele length
AssemblyAllele length
hg38161649
hg19161649
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnsv5440588, nsv6139489
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceByrska_Bishop_et_al_2022
Pubmed ID36055201
Accession Number(s)dgv339n206
Frequency
Sample Size3202
Observed Gain0
Observed Loss2
Observed Complex0
Frequencyn/a


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