A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv18179361



Internal ID20746401
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr15:89847380..89855969hg38UCSC Ensembl
chr15:90390612..90399201hg19UCSC Ensembl
Cytoband15q26.1
Allele length
AssemblyAllele length
hg388590
hg198590
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6496990
Supporting Variants
Samples
Known GenesAP3S2, C15orf38-AP3S2, MIR5094
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nssv18179361
Frequency
Sample Size19652
Observed Gain1
Observed Loss0
Observed Complex0
Frequency0


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