A curated catalogue of human genomic structural variation




Variant Details

Variant: dgv709e59



Internal ID20127458
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr11:118947883..118948045hg38UCSC Ensembl
chr11:118818593..118818755hg19UCSC Ensembl
chr11:118323803..118323965hg18UCSC Ensembl
Cytoband11q23.3
Allele length
AssemblyAllele length
hg38163
hg19163
hg18163
Variant TypeCNV tandem duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsesv3302690, esv3303036
SamplesNA11995, NA18563, NA18944, NA12891, NA18571, NA18949, NA12156, NA12828, NA18973, NA18951, NA18579, NA18572, NA18948, NA18532, NA12144, NA18945, NA12043, NA18608, NA18542, NA11881, NA18961, NA18564, NA18501, NA19102, NA19129, NA12006
Known Genes
MethodSequencing
Analysis
PlatformIllumina
Comments
Reference1000_Genomes_Consortium_Pilot_Project
Pubmed ID20981092
Accession Number(s)dgv709e59
Frequency
Sample Size185
Observed Gain26
Observed Loss0
Observed Complex0
Frequencyn/a


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