A curated catalogue of human genomic structural variation




Variant Details

Variant: dgv2622n223



Internal ID22805590
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr15:87585577..87689998hg38UCSC Ensembl
chr15:88128808..88233229hg19UCSC Ensembl
Cytoband15q25.3
Allele length
AssemblyAllele length
hg38104422
hg19104422
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnsv6500243, nsv6513841
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)dgv2622n223
Frequency
Sample Size19652
Observed Gain2
Observed Loss0
Observed Complex0
Frequencyn/a


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