A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv3237964



Internal ID22374020
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Outerchr11:91465736..91485286hg38UCSC Ensembl
Outerchr11:91198902..91218452hg19UCSC Ensembl
Cytoband11q14.3
Allele length
AssemblyAllele length
hg383389
hg193389
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv14254343
SamplesNA19238
Known Genes
MethodOptical mapping
AnalysisBioNano Genomics proprietary analysis
PlatformBioNano Genomics
Comments
ReferenceChaisson_et_al_2019
Pubmed ID30992455
Accession Number(s)nsv3237964
Frequency
Sample Size9
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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