A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv3237573



Internal ID22373909
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Outerchr11:94237004..94296385hg38UCSC Ensembl
Outerchr11:93970170..94029551hg19UCSC Ensembl
Cytoband11q21
Allele length
AssemblyAllele length
hg383846
hg193846
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv14254362
SamplesNA19238
Known Genes
MethodOptical mapping
AnalysisBioNano Genomics proprietary analysis
PlatformBioNano Genomics
Comments
ReferenceChaisson_et_al_2019
Pubmed ID30992455
Accession Number(s)nsv3237573
Frequency
Sample Size9
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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