A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv3236775



Internal ID22373687
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Outerchr11:93930292..93955448hg38UCSC Ensembl
Outerchr11:93663458..93688614hg19UCSC Ensembl
Cytoband11q21
Allele length
AssemblyAllele length
hg38814
hg19814
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv14254727, nssv14254725, nssv14254726
SamplesHG00512, NA19239, HG00513
Known Genes
MethodOptical mapping
AnalysisBioNano Genomics proprietary analysis
PlatformBioNano Genomics
Comments
ReferenceChaisson_et_al_2019
Pubmed ID30992455
Accession Number(s)nsv3236775
Frequency
Sample Size9
Observed Gain3
Observed Loss0
Observed Complex0
Frequencyn/a


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