A curated catalogue of human genomic structural variation




Variant Details

Variant: dgv1516n209



Internal ID22827591
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr3:153881419..153896196hg38UCSC Ensembl
chr3:153599208..153613985hg19UCSC Ensembl
Cytoband3q25.2
Allele length
AssemblyAllele length
hg3814778
hg1914778
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnsv5902189, nsv5895078
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)dgv1516n209
Frequency
Sample Size914
Observed Gain0
Observed Loss2
Observed Complex0
Frequencyn/a


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