A curated catalogue of human genomic structural variation




Variant Details

Variant: dgv2566n223



Internal ID22805534
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr15:65073801..65078500hg38UCSC Ensembl
chr15:65366139..65370838hg19UCSC Ensembl
Cytoband15q22.31
Allele length
AssemblyAllele length
hg384700
hg194700
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnsv6503726, nsv6501626
Samples
Known GenesKBTBD13
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)dgv2566n223
Frequency
Sample Size19652
Observed Gain2
Observed Loss0
Observed Complex0
Frequencyn/a


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