A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6496990



Internal ID20870193
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 StatusM
Merged Variants
Supporting Variantsnssv18179361
Samples
Known GenesAP3S2, C15orf38-AP3S2, MIR5094
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6496990
Frequency
Sample Size19652
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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