A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv3225284



Internal ID22368467
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Outerchr11:82134811..82290393hg38UCSC Ensembl
Outerchr11:81845853..82001435hg19UCSC Ensembl
Cytoband11q14.1
Allele length
AssemblyAllele length
hg38155583
hg19155583
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv14253545, nssv14253544
SamplesHG00732, HG00733
Known Genes
MethodOptical mapping
AnalysisBioNano Genomics proprietary analysis
PlatformBioNano Genomics
Comments
ReferenceChaisson_et_al_2019
Pubmed ID30992455
Accession Number(s)nsv3225284
Frequency
Sample Size9
Observed Gain0
Observed Loss2
Observed Complex0
Frequencyn/a


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