A curated catalogue of human genomic structural variation




Variant Details

Variant: dgv59e59



Internal ID20126808
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr1:18857271..18858969hg38UCSC Ensembl
chr1:19183765..19185463hg19UCSC Ensembl
chr1:19056352..19058050hg18UCSC Ensembl
Cytoband1p36.13
Allele length
AssemblyAllele length
hg381699
hg191699
hg181699
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsesv3403682, esv3451670, esv3348156
SamplesNA19238, NA19239, NA19240
Known GenesTAS1R2
MethodSequencing
Analysis
PlatformIllumina
Comments
Reference1000_Genomes_Consortium_Pilot_Project
Pubmed ID20981092
Accession Number(s)dgv59e59
Frequency
Sample Size185
Observed Gain3
Observed Loss0
Observed Complex0
Frequencyn/a


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