A curated catalogue of human genomic structural variation




Variant Details

Variant: dgv4500n223



Internal ID22807468
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr20:57323201..57353800hg38UCSC Ensembl
chr20:55898257..55928856hg19UCSC Ensembl
Cytoband20q13.31
Allele length
AssemblyAllele length
hg3830600
hg1930600
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnsv6543017, nsv6545069
Samples
Known GenesMIR5095, RAE1, SPO11
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)dgv4500n223
Frequency
Sample Size19652
Observed Gain2
Observed Loss0
Observed Complex0
Frequencyn/a


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