A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv3213361



Internal ID22360333
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Outerchr11:102877992..102885508hg38UCSC Ensembl
Outerchr11:102748722..102756238hg19UCSC Ensembl
Cytoband11q22.2
Allele length
AssemblyAllele length
hg387517
hg197517
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv1544n152
Supporting Variantsnssv14254448, nssv14254447
SamplesHG00512, HG00514
Known Genes
MethodOptical mapping
AnalysisBioNano Genomics proprietary analysis
PlatformBioNano Genomics
Comments
ReferenceChaisson_et_al_2019
Pubmed ID30992455
Accession Number(s)nsv3213361
Frequency
Sample Size9
Observed Gain0
Observed Loss2
Observed Complex0
Frequencyn/a


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