A curated catalogue of human genomic structural variation




Variant Details

Variant: dgv2179n223



Internal ID22805147
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr14:65869000..66498364hg38UCSC Ensembl
chr14:66335718..66965082hg19UCSC Ensembl
Cytoband14q23.3
Allele length
AssemblyAllele length
hg38629365
hg19629365
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnsv6476783, nsv6483972
Samples
Known GenesLINC00238
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)dgv2179n223
Frequency
Sample Size19652
Observed Gain2
Observed Loss0
Observed Complex0
Frequencyn/a


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