A curated catalogue of human genomic structural variation




Variant Details

Variant: esv3547690



Internal ID18402080
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr11:45111214..45111403hg38UCSC Ensembl
Outerchr11:45111183..45111445hg38UCSC Ensembl
Innerchr11:45132765..45132954hg19UCSC Ensembl
Outerchr11:45132734..45132996hg19UCSC Ensembl
Cytoband11p11.2
Allele length
AssemblyAllele length
hg38263
hg19263
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsessv9746437
Samples
Known GenesPRDM11
MethodSequencing
Analysis
PlatformIllumina HiSeq 2000
Comments
ReferenceBoomsma_et_al_2014
Pubmed ID23714750
Accession Number(s)esv3547690
Frequency
Sample Size767
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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