A curated catalogue of human genomic structural variation




Variant Details

Variant: dgv5122n223



Internal ID22808090
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr3:186376962..186379014hg38UCSC Ensembl
chr3:186094751..186096803hg19UCSC Ensembl
Cytoband3q27.3
Allele length
AssemblyAllele length
hg382053
hg192053
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnsv6364477, nsv6361807
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)dgv5122n223
Frequency
Sample Size19652
Observed Gain0
Observed Loss2
Observed Complex0
Frequencyn/a


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