A curated catalogue of human genomic structural variation




Variant Details

Variant: esv3548533



Internal ID18402923
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr11:131401799..131401849hg38UCSC Ensembl
chr11:131271694..131271744hg19UCSC Ensembl
Cytoband11q25
Allele length
AssemblyAllele length
hg3851
hg1951
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsessv9747280
Samples
Known GenesNTM
MethodSequencing
Analysis
PlatformIllumina HiSeq 2000
Comments
ReferenceBoomsma_et_al_2014
Pubmed ID23714750
Accession Number(s)esv3548533
Frequency
Sample Size767
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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