A curated catalogue of human genomic structural variation




Variant Details

Variant: dgv4427e59



Internal ID22765647
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr9:65758915..65762413hg38UCSC Ensembl
chr9:70403632..70407130hg19UCSC Ensembl
chr9:69643452..69646950hg18UCSC Ensembl
Cytoband9q12
Allele length
AssemblyAllele length
hg383499
hg193499
hg183499
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsesv3445711, esv3432333
SamplesNA19239, NA19240
Known Genes
MethodSequencing
Analysis
PlatformIllumina
Comments
Reference1000_Genomes_Consortium_Pilot_Project
Pubmed ID20981092
Accession Number(s)dgv4427e59
Frequency
Sample Size185
Observed Gain2
Observed Loss0
Observed Complex0
Frequencyn/a


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