A curated catalogue of human genomic structural variation




Variant Details

Variant: dgv4821n223



Internal ID22807789
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr3:22629521..22735201hg38UCSC Ensembl
chr3:22671012..22776692hg19UCSC Ensembl
Cytoband3p24.3
Allele length
AssemblyAllele length
hg38105681
hg19105681
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnsv6371577, nsv6371436
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)dgv4821n223
Frequency
Sample Size19652
Observed Gain2
Observed Loss0
Observed Complex0
Frequencyn/a


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