A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv3211238



Internal ID22358860
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Outerchr11:11657215..11693573hg38UCSC Ensembl
Outerchr11:11678762..11715120hg19UCSC Ensembl
Cytoband11p15.3
Allele length
AssemblyAllele length
hg3836359
hg1936359
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv14253851
SamplesNA19239
Known Genes
MethodOptical mapping
AnalysisBioNano Genomics proprietary analysis
PlatformBioNano Genomics
Comments
ReferenceChaisson_et_al_2019
Pubmed ID30992455
Accession Number(s)nsv3211238
Frequency
Sample Size9
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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