A curated catalogue of human genomic structural variation




Variant Details

Variant: dgv1288n209



Internal ID22827363
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr20:28835603..29200052hg38UCSC Ensembl
Cytoband
Allele length
AssemblyAllele length
hg38364450
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnsv5963622, nsv5963484, nsv5955330, nsv5956206, nsv5959373, nsv5952671, nsv5955720, nsv5947614, nsv5949711, nsv5954153, nsv5950972, nsv5949795
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)dgv1288n209
Frequency
Sample Size914
Observed Gain0
Observed Loss12
Observed Complex0
Frequencyn/a


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