A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv3212822



Internal ID22359957
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Outerchr11:6157298..6175807hg38UCSC Ensembl
Outerchr11:6178528..6197037hg19UCSC Ensembl
Cytoband11p15.4
Allele length
AssemblyAllele length
hg3818510
hg1918510
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv14253848
SamplesNA19239
Known GenesOR52B2
MethodOptical mapping
AnalysisBioNano Genomics proprietary analysis
PlatformBioNano Genomics
Comments
ReferenceChaisson_et_al_2019
Pubmed ID30992455
Accession Number(s)nsv3212822
Frequency
Sample Size9
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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