A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv3219319



Internal ID22364373
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Outerchr11:93763661..93784474hg38UCSC Ensembl
Outerchr11:93496827..93517640hg19UCSC Ensembl
Cytoband11q21
Allele length
AssemblyAllele length
hg3820814
hg1920814
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv14253599
SamplesNA19238
Known GenesMED17
MethodOptical mapping
AnalysisBioNano Genomics proprietary analysis
PlatformBioNano Genomics
Comments
ReferenceChaisson_et_al_2019
Pubmed ID30992455
Accession Number(s)nsv3219319
Frequency
Sample Size9
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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