A curated catalogue of human genomic structural variation




Variant Details

Variant: dgv2645n223



Internal ID22805613
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr15:98645201..98652100hg38UCSC Ensembl
chr15:99188430..99195329hg19UCSC Ensembl
Cytoband15q26.3
Allele length
AssemblyAllele length
hg386900
hg196900
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnsv6496128, nsv6505450
Samples
Known GenesIGF1R
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)dgv2645n223
Frequency
Sample Size19652
Observed Gain2
Observed Loss0
Observed Complex0
Frequencyn/a


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