A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv3226351



Internal ID22369186
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Outerchr13:21841139..21860135hg38UCSC Ensembl
Outerchr13:22415278..22434274hg19UCSC Ensembl
Cytoband13q12.11
Allele length
AssemblyAllele length
hg3818997
hg1918997
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv14257037
SamplesNA19238
Known Genes
MethodOptical mapping
AnalysisBioNano Genomics proprietary analysis
PlatformBioNano Genomics
Comments
ReferenceChaisson_et_al_2019
Pubmed ID30992455
Accession Number(s)nsv3226351
Frequency
Sample Size9
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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