A curated catalogue of human genomic structural variation




Variant Details

Variant: dgv2059n223



Internal ID22805027
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr14:21581801..21590900hg38UCSC Ensembl
chr14:22049936..22059019hg19UCSC Ensembl
Cytoband14q11.2
Allele length
AssemblyAllele length
hg389100
hg199084
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnsv6487329, nsv6478286
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)dgv2059n223
Frequency
Sample Size19652
Observed Gain2
Observed Loss0
Observed Complex0
Frequencyn/a


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