A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv3220787



Internal ID22365386
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Outerchr13:86501227..86573354hg38UCSC Ensembl
Outerchr13:87153482..87225609hg19UCSC Ensembl
Cytoband13q31.1
Allele length
AssemblyAllele length
hg3872128
hg1972128
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv14256950
SamplesHG00513
Known Genes
MethodOptical mapping
AnalysisBioNano Genomics proprietary analysis
PlatformBioNano Genomics
Comments
ReferenceChaisson_et_al_2019
Pubmed ID30992455
Accession Number(s)nsv3220787
Frequency
Sample Size9
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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