A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv3235713



Internal ID22373373
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Outerchr11:94188339..94250475hg38UCSC Ensembl
Outerchr11:93921505..93983641hg19UCSC Ensembl
Cytoband11q21
Allele length
AssemblyAllele length
hg3813071
hg1913071
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv14254948
SamplesHG00514
Known Genes
MethodOptical mapping
AnalysisBioNano Genomics proprietary analysis
PlatformBioNano Genomics
Comments
ReferenceChaisson_et_al_2019
Pubmed ID30992455
Accession Number(s)nsv3235713
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