A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6590469



Internal ID20963540
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 StatusM
Merged Variants
Supporting Variantsnssv18240548
Samples
Known GenesANPEP, AP3S2, C15orf38, C15orf38-AP3S2, MESP1, MESP2, MIR5094, WDR93
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6590469
Frequency
Sample Size19652
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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