A curated catalogue of human genomic structural variation




Variant Details

Variant: dgv5070n223



Internal ID22808038
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr3:165545401..165578816hg38UCSC Ensembl
chr3:165263189..165296604hg19UCSC Ensembl
Cytoband3q26.1
Allele length
AssemblyAllele length
hg3833416
hg1933416
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnsv6368542, nsv6362210
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)dgv5070n223
Frequency
Sample Size19652
Observed Gain0
Observed Loss2
Observed Complex0
Frequencyn/a


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