A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv3221823



Internal ID22366081
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Outerchr11:1626181..1643713hg38UCSC Ensembl
Outerchr11:1647411..1664943hg19UCSC Ensembl
Cytoband11p15.5
Allele length
AssemblyAllele length
hg3817533
hg1917533
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv14253512
SamplesHG00731
Known GenesKRTAP5-5, MOB2
MethodOptical mapping
AnalysisBioNano Genomics proprietary analysis
PlatformBioNano Genomics
Comments
ReferenceChaisson_et_al_2019
Pubmed ID30992455
Accession Number(s)nsv3221823
Frequency
Sample Size9
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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