A curated catalogue of human genomic structural variation




Variant Details

Variant: esv3547262



Internal ID18748338
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr11:5765218..5786654hg38UCSC Ensembl
Outerchr11:5761406..5788699hg38UCSC Ensembl
Innerchr11:5786448..5807884hg19UCSC Ensembl
Outerchr11:5782636..5809929hg19UCSC Ensembl
Cytoband11p15.4
Allele length
AssemblyAllele length
hg3827294
hg1927294
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsessv9746009
Samples
Known GenesOR52N1, OR52N5
MethodSequencing
Analysis
PlatformIllumina HiSeq 2000
Comments
ReferenceBoomsma_et_al_2014
Pubmed ID23714750
Accession Number(s)esv3547262
Frequency
Sample Size767
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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