A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv3226635



Internal ID22369369
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Outerchr15:49246985..49263671hg38UCSC Ensembl
Outerchr15:49539182..49555868hg19UCSC Ensembl
Cytoband15q21.2
Allele length
AssemblyAllele length
hg3816687
hg1916687
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv14257916, nssv14257915
SamplesNA19239, NA19240
Known GenesGALK2
MethodOptical mapping
AnalysisBioNano Genomics proprietary analysis
PlatformBioNano Genomics
Comments
ReferenceChaisson_et_al_2019
Pubmed ID30992455
Accession Number(s)nsv3226635
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