A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv3222964



Internal ID22366869
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Outerchr11:1128585..1167951hg38UCSC Ensembl
Outerchr11:1122493..1161286hg19UCSC Ensembl
Cytoband11p15.5
Allele length
AssemblyAllele length
hg3839367
hg1938794
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv14254432, nssv14254431
SamplesHG00512, HG00514
Known Genes
MethodOptical mapping
AnalysisBioNano Genomics proprietary analysis
PlatformBioNano Genomics
Comments
ReferenceChaisson_et_al_2019
Pubmed ID30992455
Accession Number(s)nsv3222964
Frequency
Sample Size9
Observed Gain0
Observed Loss2
Observed Complex0
Frequencyn/a


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