A curated catalogue of human genomic structural variation




Variant Details

Variant: dgv4843n223



Internal ID22807811
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr3:35761401..35902800hg38UCSC Ensembl
chr3:35802893..35944292hg19UCSC Ensembl
Cytoband3p22.3
Allele length
AssemblyAllele length
hg38141400
hg19141400
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnsv6360375, nsv6369120, nsv6374265, nsv6374880
Samples
Known GenesARPP21
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)dgv4843n223
Frequency
Sample Size19652
Observed Gain4
Observed Loss0
Observed Complex0
Frequencyn/a


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