A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv18240548



Internal ID20807588
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr15:89731371..89910439hg38UCSC Ensembl
chr15:90274602..90453671hg19UCSC Ensembl
Cytoband15q26.1
Allele length
AssemblyAllele length
hg38179069
hg19179070
Variant TypeOTHER inversion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6590469
Supporting Variants
Samples
Known GenesANPEP, AP3S2, C15orf38, C15orf38-AP3S2, MESP1, MESP2, MIR5094, WDR93
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nssv18240548
Frequency
Sample Size19652
Observed Gain0
Observed Loss0
Observed Complex0
Frequency0


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