A curated catalogue of human genomic structural variation




Variant Details

Variant: esv3548549



Internal ID18402939
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr11:133122606..133133393hg38UCSC Ensembl
Outerchr11:133122106..133135105hg38UCSC Ensembl
Innerchr11:132992501..133003288hg19UCSC Ensembl
Outerchr11:132992001..133005000hg19UCSC Ensembl
Cytoband11q25
Allele length
AssemblyAllele length
hg3813000
hg1913000
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsessv9747296
Samples
Known GenesOPCML
MethodSequencing
Analysis
PlatformIllumina HiSeq 2000
Comments
ReferenceBoomsma_et_al_2014
Pubmed ID23714750
Accession Number(s)esv3548549
Frequency
Sample Size767
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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