A curated catalogue of human genomic structural variation




Variant Details

Variant: dgv2886n223



Internal ID22805854
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr16:55808001..55812300hg38UCSC Ensembl
chr16:55841913..55846212hg19UCSC Ensembl
Cytoband16q12.2
Allele length
AssemblyAllele length
hg384300
hg194300
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnsv6503224, nsv6505973
Samples
Known GenesCES1
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)dgv2886n223
Frequency
Sample Size19652
Observed Gain2
Observed Loss0
Observed Complex0
Frequencyn/a


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