A curated catalogue of human genomic structural variation




Variant Details

Variant: dgv2082n223



Internal ID22805050
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr14:27338288..27422109hg38UCSC Ensembl
chr14:27807494..27891315hg19UCSC Ensembl
Cytoband14q12
Allele length
AssemblyAllele length
hg3883822
hg1983822
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnsv6483408, nsv6484962
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)dgv2082n223
Frequency
Sample Size19652
Observed Gain0
Observed Loss2
Observed Complex0
Frequencyn/a


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