A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv3223413



Internal ID22367190
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Outerchr11:76425967..76442539hg38UCSC Ensembl
Outerchr11:76137011..76153583hg19UCSC Ensembl
Cytoband11q13.5
Allele length
AssemblyAllele length
hg3816573
hg1916573
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv14253067
SamplesNA19238
Known Genes
MethodOptical mapping
AnalysisBioNano Genomics proprietary analysis
PlatformBioNano Genomics
Comments
ReferenceChaisson_et_al_2019
Pubmed ID30992455
Accession Number(s)nsv3223413
Frequency
Sample Size9
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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