A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv3211508



Internal ID22359046
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Outerchr11:11785603..11806219hg38UCSC Ensembl
Outerchr11:11807150..11827766hg19UCSC Ensembl
Cytoband11p15.3
Allele length
AssemblyAllele length
hg3820617
hg1920617
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv1270n152
Supporting Variantsnssv14253517
SamplesHG00731
Known Genes
MethodOptical mapping
AnalysisBioNano Genomics proprietary analysis
PlatformBioNano Genomics
Comments
ReferenceChaisson_et_al_2019
Pubmed ID30992455
Accession Number(s)nsv3211508
Frequency
Sample Size9
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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