A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv3225289



Internal ID22368471
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Outerchr11:81914366..81991218hg38UCSC Ensembl
Outerchr11:81625408..81702260hg19UCSC Ensembl
Cytoband11q14.1
Allele length
AssemblyAllele length
hg3876853
hg1976853
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv14254212
SamplesHG00733
Known Genes
MethodOptical mapping
AnalysisBioNano Genomics proprietary analysis
PlatformBioNano Genomics
Comments
ReferenceChaisson_et_al_2019
Pubmed ID30992455
Accession Number(s)nsv3225289
Frequency
Sample Size9
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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