A curated catalogue of human genomic structural variation




Variant Details

Variant: dgv7e59



Internal ID22761227
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr1:260138..269036hg38UCSC Ensembl
chr1:229889..238787hg19UCSC Ensembl
chr1:219752..228650hg18UCSC Ensembl
Cytoband1p36.33
Allele length
AssemblyAllele length
hg388899
hg198899
hg188899
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsesv3431827, esv3432331, esv3413313
SamplesNA19239, NA12878, NA19240
Known Genes
MethodSequencing
Analysis
PlatformIllumina
Comments
Reference1000_Genomes_Consortium_Pilot_Project
Pubmed ID20981092
Accession Number(s)dgv7e59
Frequency
Sample Size185
Observed Gain3
Observed Loss0
Observed Complex0
Frequencyn/a


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