A curated catalogue of human genomic structural variation




Variant Details

Variant: dgv14e59



Internal ID20126763
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr1:1029709..1031607hg38UCSC Ensembl
chr1:965089..966987hg19UCSC Ensembl
chr1:954952..956850hg18UCSC Ensembl
Cytoband1p36.33
Allele length
AssemblyAllele length
hg381899
hg191899
hg181899
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsesv3441341, esv3385140
SamplesNA19239, NA19240
Known GenesAGRN
MethodSequencing
Analysis
PlatformIllumina
Comments
Reference1000_Genomes_Consortium_Pilot_Project
Pubmed ID20981092
Accession Number(s)dgv14e59
Frequency
Sample Size185
Observed Gain2
Observed Loss0
Observed Complex0
Frequencyn/a


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