A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6028555



Internal ID21937898
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr15:89853535..89867642hg38UCSC Ensembl
chr15:90396767..90410874hg19UCSC Ensembl
Cytoband15q26.1
Allele length
AssemblyAllele length
hg3814108
hg1914108
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17602620
Samples
Known GenesAP3S2, C15orf38-AP3S2
MethodSequencing
Analysis
Platform
Comments
ReferenceWu_et_al_2021
Pubmed ID34764282
Accession Number(s)nsv6028555
Frequency
Sample Size405
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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