A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv3225182



Internal ID22368388
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Outerchr11:4354280..4418331hg38UCSC Ensembl
Outerchr11:4375510..4439561hg19UCSC Ensembl
Cytoband11p15.4
Allele length
AssemblyAllele length
hg3864052
hg1964052
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv14253535
SamplesHG00732
Known GenesOR52B4, TRIM21
MethodOptical mapping
AnalysisBioNano Genomics proprietary analysis
PlatformBioNano Genomics
Comments
ReferenceChaisson_et_al_2019
Pubmed ID30992455
Accession Number(s)nsv3225182
Frequency
Sample Size9
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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