A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv18240549



Internal ID20807589
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr15:89842906..89843393hg38UCSC Ensembl
chr15:90386138..90386625hg19UCSC Ensembl
Cytoband15q26.1
Allele length
AssemblyAllele length
hg38488
hg19488
Variant TypeOTHER inversion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6580720
Supporting Variants
Samples
Known GenesAP3S2, C15orf38-AP3S2
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nssv18240549
Frequency
Sample Size19652
Observed Gain0
Observed Loss0
Observed Complex0
Frequency0.00017


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