A curated catalogue of human genomic structural variation




Variant Details

Variant: dgv4856n223



Internal ID22807824
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr3:43276501..43294000hg38UCSC Ensembl
chr3:43317993..43335492hg19UCSC Ensembl
Cytoband3p22.1
Allele length
AssemblyAllele length
hg3817500
hg1917500
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnsv6359125, nsv6355994
Samples
Known GenesSNRK
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)dgv4856n223
Frequency
Sample Size19652
Observed Gain2
Observed Loss0
Observed Complex0
Frequencyn/a


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