A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6029389



Internal ID21938732
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr15:59527351..59550561hg38UCSC Ensembl
chr15:59819550..59842760hg19UCSC Ensembl
Cytoband15q22.2
Allele length
AssemblyAllele length
hg3823211
hg1923211
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17612372
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceWu_et_al_2021
Pubmed ID34764282
Accession Number(s)nsv6029389
Frequency
Sample Size405
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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