A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv3241826



Internal ID22375081
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Outerchr11:110492238..110510654hg38UCSC Ensembl
Outerchr11:110362962..110381378hg19UCSC Ensembl
Cytoband11q22.3
Allele length
AssemblyAllele length
hg386030
hg196030
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv14255723, nssv14255724, nssv14255726, nssv14255725, nssv14255727
SamplesHG00512, HG00731, HG00732, HG00513, HG00514
Known Genes
MethodOptical mapping
AnalysisBioNano Genomics proprietary analysis
PlatformBioNano Genomics
Comments
ReferenceChaisson_et_al_2019
Pubmed ID30992455
Accession Number(s)nsv3241826
Frequency
Sample Size9
Observed Gain5
Observed Loss0
Observed Complex0
Frequencyn/a


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