A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv3238179



Internal ID22374087
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 State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv14261848, nssv14261844, nssv14261850, nssv14261852, nssv14261851, nssv14261849, nssv14261846, nssv14261845, nssv14261847
SamplesHG00512, NA19238, NA19239, HG00731, HG00732, NA19240, HG00733, HG00513, HG00514
Known Genes
MethodOptical mapping
AnalysisBioNano Genomics proprietary analysis
PlatformBioNano Genomics
Comments
ReferenceChaisson_et_al_2019
Pubmed ID30992455
Accession Number(s)nsv3238179
Frequency
Sample Size9
Observed Gain9
Observed Loss0
Observed Complex0
Frequencyn/a


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