A curated catalogue of human genomic structural variation




Variant Details

Variant: dgv4844n223



Internal ID22807812
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr3:35761501..35822200hg38UCSC Ensembl
chr3:35802993..35863692hg19UCSC Ensembl
Cytoband3p22.3
Allele length
AssemblyAllele length
hg3860700
hg1960700
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnsv6363421, nsv6357661, nsv6366711
Samples
Known GenesARPP21
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)dgv4844n223
Frequency
Sample Size19652
Observed Gain3
Observed Loss0
Observed Complex0
Frequencyn/a


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