A curated catalogue of human genomic structural variation




Variant Details

Variant: esv3187477



Internal ID10860457
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr14:102813141..102813226hg38UCSC Ensembl
chr14:103279478..103279563hg19UCSC Ensembl
Cytoband14q32.32
Allele length
AssemblyAllele length
hg3886
hg1986
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsessv7457044
SamplesHuRef
Known GenesTRAF3
MethodSequencing
Analysis
PlatformComplete Genomics
Comments
ReferencePang_et_al_2013b
Pubmed ID24192839
Accession Number(s)esv3187477
Frequency
Sample Size1
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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