A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1154779



Internal ID22085284
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr11:124216204..124225350hg38UCSC Ensembl
Outerchr11:124215715..124232096hg38UCSC Ensembl
Innerchr11:124086911..124096055hg19UCSC Ensembl
Outerchr11:124086422..124102798hg19UCSC Ensembl
Cytoband11q24.2
Allele length
AssemblyAllele length
hg3816382
hg1916377
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv54n97
Supporting Variantsnssv4007319
Samples
Known GenesOR8G2
MethodSNP array
AnalysisDefault settings
Platform
Comments
ReferenceLou_et_al_2014
Pubmed ID25026903
Accession Number(s)nsv1154779
Frequency
Sample Size131
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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