A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv3216089



Internal ID22362205
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Outerchr11:42777112..42820577hg38UCSC Ensembl
Outerchr11:42798662..42842127hg19UCSC Ensembl
Cytoband11p12
Allele length
AssemblyAllele length
hg3843466
hg1943466
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv14253521
SamplesHG00731
Known Genes
MethodOptical mapping
AnalysisBioNano Genomics proprietary analysis
PlatformBioNano Genomics
Comments
ReferenceChaisson_et_al_2019
Pubmed ID30992455
Accession Number(s)nsv3216089
Frequency
Sample Size9
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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