A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv14261850



Internal ID22265770
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Outerchr18:22445562..22463346hg38UCSC Ensembl
Outerchr18:20025525..20043309hg19UCSC Ensembl
Cytoband18q11.2
Allele length
AssemblyAllele length
hg38889
hg19889
Variant TypeCNV insertion
Copy Number
Allele StateHomozygous
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv3238179
Supporting Variants
SamplesNA19238
Known Genes
MethodOptical mapping
AnalysisBioNano Genomics proprietary analysis
PlatformBioNano Genomics
Comments
ReferenceChaisson_et_al_2019
Pubmed ID30992455
Accession Number(s)nssv14261850
Frequency
Sample Size9
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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