A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv3230017



Internal ID22371675
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Outerchr9:39798212..41547356hg38UCSC Ensembl
Cytoband
Allele length
AssemblyAllele length
hg381749145
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv14281668
SamplesNA19238
Known Genes
MethodOptical mapping
AnalysisBioNano Genomics proprietary analysis
PlatformBioNano Genomics
Comments
ReferenceChaisson_et_al_2019
Pubmed ID30992455
Accession Number(s)nsv3230017
Frequency
Sample Size9
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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