A curated catalogue of human genomic structural variation




Variant Details

Variant: dgv2116n223



Internal ID22805084
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr14:42667401..43032200hg38UCSC Ensembl
chr14:43136604..43501403hg19UCSC Ensembl
Cytoband14q21.1
Allele length
AssemblyAllele length
hg38364800
hg19364800
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnsv6495027, nsv6481438
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)dgv2116n223
Frequency
Sample Size19652
Observed Gain2
Observed Loss0
Observed Complex0
Frequencyn/a


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