A curated catalogue of human genomic structural variation




Variant Details

Variant: dgv2942n223



Internal ID22805910
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr16:77893031..78630216hg38UCSC Ensembl
chr16:77926928..78664113hg19UCSC Ensembl
Cytoband16q23.1
Allele length
AssemblyAllele length
hg38737186
hg19737186
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnsv6515467, nsv6501096
Samples
Known GenesCLEC3A, VAT1L, WWOX
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)dgv2942n223
Frequency
Sample Size19652
Observed Gain2
Observed Loss0
Observed Complex0
Frequencyn/a


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