A curated catalogue of human genomic structural variation




Variant Details

Variant: dgv715e59



Internal ID20127464
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr11:126226047..126226545hg38UCSC Ensembl
chr11:126095942..126096440hg19UCSC Ensembl
chr11:125601152..125601650hg18UCSC Ensembl
Cytoband11q24.2
Allele length
AssemblyAllele length
hg38499
hg19499
hg18499
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsesv3334212, esv3410389, esv3352173, esv3448290, esv3441476
SamplesNA12891, NA19238, NA19239, NA12878, NA19240
Known GenesFAM118B
MethodSequencing
Analysis
PlatformIllumina
Comments
Reference1000_Genomes_Consortium_Pilot_Project
Pubmed ID20981092
Accession Number(s)dgv715e59
Frequency
Sample Size185
Observed Gain5
Observed Loss0
Observed Complex0
Frequencyn/a


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