A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv3226098



Internal ID22369022
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Outerchr15:91404734..91459392hg38UCSC Ensembl
Outerchr15:91947964..92002622hg19UCSC Ensembl
Cytoband15q26.1
Allele length
AssemblyAllele length
hg3854659
hg1954659
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv14258512, nssv14258511
SamplesHG00732, HG00733
Known Genes
MethodOptical mapping
AnalysisBioNano Genomics proprietary analysis
PlatformBioNano Genomics
Comments
ReferenceChaisson_et_al_2019
Pubmed ID30992455
Accession Number(s)nsv3226098
Frequency
Sample Size9
Observed Gain0
Observed Loss2
Observed Complex0
Frequencyn/a


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