A curated catalogue of human genomic structural variation




Variant Details

Variant: dgv2081n223



Internal ID22805049
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr14:27280081..27372831hg38UCSC Ensembl
chr14:27749287..27842037hg19UCSC Ensembl
Cytoband14q12
Allele length
AssemblyAllele length
hg3892751
hg1992751
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnsv6479922, nsv6479075
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)dgv2081n223
Frequency
Sample Size19652
Observed Gain0
Observed Loss2
Observed Complex0
Frequencyn/a


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