A curated catalogue of human genomic structural variation




Variant Details

Variant: essv9750832



Internal ID18378392
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Cytoband14q32.32
Allele length
AssemblyAllele length
hg1955
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsesv3552085
Supporting Variants
Samples
Known GenesTRAF3
MethodSequencing
Analysis
PlatformIllumina HiSeq 2000
Comments
ReferenceBoomsma_et_al_2014
Pubmed ID23714750
Accession Number(s)essv9750832
Frequency
Sample Size767
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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