A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv3225106



Internal ID22368336
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Outerchr18:18259384..20926650hg38UCSC Ensembl
Cytoband
Allele length
AssemblyAllele length
hg382667267
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv3784n152
Supporting Variantsnssv14261744
SamplesHG00514
Known Genes
MethodOptical mapping
AnalysisBioNano Genomics proprietary analysis
PlatformBioNano Genomics
Comments
ReferenceChaisson_et_al_2019
Pubmed ID30992455
Accession Number(s)nsv3225106
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