A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv3246417



Internal ID22376405
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Outerchr13:26966047..26975018hg38UCSC Ensembl
Outerchr13:27540184..27549155hg19UCSC Ensembl
Cytoband13q12.13
Allele length
AssemblyAllele length
hg381245
hg191245
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv14257284, nssv14256634, nssv14257283, nssv14257285, nssv14256636, nssv14257282, nssv14256637, nssv14256633, nssv14256635
SamplesHG00512, NA19238, NA19239, HG00731, HG00732, NA19240, HG00733, HG00513, HG00514
Known Genes
MethodOptical mapping
AnalysisBioNano Genomics proprietary analysis
PlatformBioNano Genomics
Comments
ReferenceChaisson_et_al_2019
Pubmed ID30992455
Accession Number(s)nsv3246417
Frequency
Sample Size9
Observed Gain9
Observed Loss0
Observed Complex0
Frequencyn/a


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