A curated catalogue of human genomic structural variation




Variant Details

Variant: esv3548537



Internal ID18402927
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr11:132069280..132070186hg38UCSC Ensembl
Outerchr11:132069092..132070347hg38UCSC Ensembl
Innerchr11:131939174..131940080hg19UCSC Ensembl
Outerchr11:131938986..131940241hg19UCSC Ensembl
Cytoband11q25
Allele length
AssemblyAllele length
hg381256
hg191256
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsessv9747284
Samples
Known GenesNTM
MethodSequencing
Analysis
PlatformIllumina HiSeq 2000
Comments
ReferenceBoomsma_et_al_2014
Pubmed ID23714750
Accession Number(s)esv3548537
Frequency
Sample Size767
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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