A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv3217336



Internal ID22363033
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Outerchr18:35771359..35850560hg38UCSC Ensembl
Outerchr18:33351323..33430524hg19UCSC Ensembl
Cytoband18q12.2
Allele length
AssemblyAllele length
hg3879202
hg1979202
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv14261764
SamplesHG00731
Known Genes
MethodOptical mapping
AnalysisBioNano Genomics proprietary analysis
PlatformBioNano Genomics
Comments
ReferenceChaisson_et_al_2019
Pubmed ID30992455
Accession Number(s)nsv3217336
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