A curated catalogue of human genomic structural variation




Variant Details

Variant: dgv1111e59



Internal ID22762331
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr13:109293103..109295201hg38UCSC Ensembl
chr13:109945451..109947549hg19UCSC Ensembl
chr13:108743452..108745550hg18UCSC Ensembl
Cytoband13q33.3
Allele length
AssemblyAllele length
hg382099
hg192099
hg182099
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsesv3414437, esv3335971, esv3400884
SamplesNA19238, NA19239, NA19240
Known Genes
MethodSequencing
Analysis
PlatformIllumina
Comments
Reference1000_Genomes_Consortium_Pilot_Project
Pubmed ID20981092
Accession Number(s)dgv1111e59
Frequency
Sample Size185
Observed Gain3
Observed Loss0
Observed Complex0
Frequencyn/a


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