A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1154757



Internal ID22085262
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr11:90098873..90124386hg38UCSC Ensembl
Outerchr11:90085436..90135587hg38UCSC Ensembl
Innerchr11:89832041..89857554hg19UCSC Ensembl
Outerchr11:89818604..89868755hg19UCSC Ensembl
Cytoband11q14.3
Allele length
AssemblyAllele length
hg3850152
hg1950152
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv4007236
Samples
Known GenesNAALAD2, UBTFL1
MethodSNP array
AnalysisDefault settings
Platform
Comments
ReferenceLou_et_al_2014
Pubmed ID25026903
Accession Number(s)nsv1154757
Frequency
Sample Size131
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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