A curated catalogue of human genomic structural variation




Variant Details

Variant: dgv1339e59



Internal ID22762559
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr14:105229570..105240968hg38UCSC Ensembl
chr14:105695907..105707305hg19UCSC Ensembl
chr14:104766952..104778350hg18UCSC Ensembl
Cytoband14q32.33
Allele length
AssemblyAllele length
hg3811399
hg1911399
hg1811399
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsesv3359991, esv3441758, esv3428308
SamplesNA19238, NA19239, NA19240
Known GenesBRF1
MethodSequencing
Analysis
PlatformIllumina
Comments
Reference1000_Genomes_Consortium_Pilot_Project
Pubmed ID20981092
Accession Number(s)dgv1339e59
Frequency
Sample Size185
Observed Gain3
Observed Loss0
Observed Complex0
Frequencyn/a


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