A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv3236858



Internal ID22373712
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Outerchr11:69215204..69217057hg38UCSC Ensembl
Outerchr11:68982671..68984524hg19UCSC Ensembl
Cytoband11q13.3
Allele length
AssemblyAllele length
hg381002
hg191002
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv14255111, nssv14255110
SamplesNA19238, HG00733
Known Genes
MethodOptical mapping
AnalysisBioNano Genomics proprietary analysis
PlatformBioNano Genomics
Comments
ReferenceChaisson_et_al_2019
Pubmed ID30992455
Accession Number(s)nsv3236858
Frequency
Sample Size9
Observed Gain2
Observed Loss0
Observed Complex0
Frequencyn/a


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