A curated catalogue of human genomic structural variation




Variant Details

Variant: dgv4419n223



Internal ID22807387
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr20:16579501..16584761hg38UCSC Ensembl
chr20:16560146..16565406hg19UCSC Ensembl
Cytoband20p12.1
Allele length
AssemblyAllele length
hg385261
hg195261
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnsv6531535, nsv6533232
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)dgv4419n223
Frequency
Sample Size19652
Observed Gain0
Observed Loss2
Observed Complex0
Frequencyn/a


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