A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv3226381



Internal ID22369204
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Outerchr9:33209658..33223508hg38UCSC Ensembl
Outerchr9:33209656..33223506hg19UCSC Ensembl
Cytoband9p13.3
Allele length
AssemblyAllele length
hg3813851
hg1913851
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv14282847, nssv14282846
SamplesHG00513, HG00514
Known Genes
MethodOptical mapping
AnalysisBioNano Genomics proprietary analysis
PlatformBioNano Genomics
Comments
ReferenceChaisson_et_al_2019
Pubmed ID30992455
Accession Number(s)nsv3226381
Frequency
Sample Size9
Observed Gain0
Observed Loss2
Observed Complex0
Frequencyn/a


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