A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv3214915



Internal ID22361418
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Outerchr11:86568669..86618942hg38UCSC Ensembl
Outerchr11:86279711..86329984hg19UCSC Ensembl
Cytoband11q14.2
Allele length
AssemblyAllele length
hg3850274
hg1950274
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv14253509
SamplesHG00514
Known GenesME3
MethodOptical mapping
AnalysisBioNano Genomics proprietary analysis
PlatformBioNano Genomics
Comments
ReferenceChaisson_et_al_2019
Pubmed ID30992455
Accession Number(s)nsv3214915
Frequency
Sample Size9
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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