A curated catalogue of human genomic structural variation




Variant Details

Variant: dgv2885n223



Internal ID22805853
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr16:55807201..55822500hg38UCSC Ensembl
chr16:55841113..55856412hg19UCSC Ensembl
Cytoband16q12.2
Allele length
AssemblyAllele length
hg3815300
hg1915300
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnsv6504479, nsv6508974, nsv6513884, nsv6501783
Samples
Known GenesCES1
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)dgv2885n223
Frequency
Sample Size19652
Observed Gain4
Observed Loss0
Observed Complex0
Frequencyn/a


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