A curated catalogue of human genomic structural variation




Variant Details

Variant: dgv4473e59



Internal ID22765693
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr9:89058017..89061415hg38UCSC Ensembl
chr9:91672932..91676330hg19UCSC Ensembl
chr9:90862752..90866150hg18UCSC Ensembl
Cytoband9q22.1
Allele length
AssemblyAllele length
hg383399
hg193399
hg183399
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsesv3341868, esv3427865
SamplesNA19239, NA19240
Known GenesSHC3
MethodSequencing
Analysis
PlatformIllumina
Comments
Reference1000_Genomes_Consortium_Pilot_Project
Pubmed ID20981092
Accession Number(s)dgv4473e59
Frequency
Sample Size185
Observed Gain2
Observed Loss0
Observed Complex0
Frequencyn/a


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