A curated catalogue of human genomic structural variation




Variant Details

Variant: esv3550219



Internal ID18751295
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Cytoband13q12.13
Allele length
AssemblyAllele length
hg1969
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv99e215
Supporting Variantsessv9748966
Samples
Known Genes
MethodSequencing
Analysis
PlatformIllumina HiSeq 2000
Comments
ReferenceBoomsma_et_al_2014
Pubmed ID23714750
Accession Number(s)esv3550219
Frequency
Sample Size767
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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