A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6588997



Internal ID20962068
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr15:89885202..89885936hg38UCSC Ensembl
chr15:90428434..90429168hg19UCSC Ensembl
Cytoband15q26.1
Allele length
AssemblyAllele length
hg38735
hg19735
Variant TypeOTHER inversion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv2623n223
Supporting Variantsnssv18240551
Samples
Known GenesAP3S2, C15orf38-AP3S2
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6588997
Frequency
Sample Size19652
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


Hosted by The Centre for Applied Genomics
Grant support for DGV
Please read the usage disclaimer