A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv3213363



Internal ID22360335
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr9:124784823..124784971hg38UCSC Ensembl
chr9:127547102..127547250hg19UCSC Ensembl
Cytoband9q33.3
Allele length
AssemblyAllele length
hg38149
hg19149
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv14347689, nssv14347690
SamplesHG00513, HG00514
Known GenesOLFML2A
MethodSequencing
AnalysisMultiple analysis algorthms
PlatformIllumina HiSeq
Comments
ReferenceChaisson_et_al_2019
Pubmed ID30992455
Accession Number(s)nsv3213363
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