A curated catalogue of human genomic structural variation




Variant Details

Variant: dgv4508n223



Internal ID22807476
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr20:64316801..64327500hg38UCSC Ensembl
chr20:62948154..62958853hg19UCSC Ensembl
Cytoband20q13.33
Allele length
AssemblyAllele length
hg3810700
hg1910700
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnsv6548514, nsv6546166
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)dgv4508n223
Frequency
Sample Size19652
Observed Gain2
Observed Loss0
Observed Complex0
Frequencyn/a


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