A curated catalogue of human genomic structural variation




Variant Details

Variant: dgv4273e59



Internal ID22765493
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr9:29452..36550hg38UCSC Ensembl
chr9:29452..36550hg19UCSC Ensembl
chr9:19452..26550hg18UCSC Ensembl
Cytoband9p24.3
Allele length
AssemblyAllele length
hg387099
hg197099
hg187099
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsesv3347609, esv3366630, esv3353764
SamplesNA19239, NA12878, NA12892
Known GenesFAM138C, WASH1
MethodSequencing
Analysis
PlatformIllumina
Comments
Reference1000_Genomes_Consortium_Pilot_Project
Pubmed ID20981092
Accession Number(s)dgv4273e59
Frequency
Sample Size185
Observed Gain3
Observed Loss0
Observed Complex0
Frequencyn/a


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