A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv3211868



Internal ID22359289
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Outerchr11:87866917..87888614hg38UCSC Ensembl
Outerchr11:87577809..87599506hg19UCSC Ensembl
Cytoband11q14.2
Allele length
AssemblyAllele length
hg3821698
hg1921698
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv14254213
SamplesHG00733
Known Genes
MethodOptical mapping
AnalysisBioNano Genomics proprietary analysis
PlatformBioNano Genomics
Comments
ReferenceChaisson_et_al_2019
Pubmed ID30992455
Accession Number(s)nsv3211868
Frequency
Sample Size9
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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