A curated catalogue of human genomic structural variation




Variant Details

Variant: dgv4373e59



Internal ID22765593
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr9:62407855..62417953hg38UCSC Ensembl
chr9:46719156..46729254hg19UCSC Ensembl
chr9:46559152..46569250hg18UCSC Ensembl
Cytoband9p11.2
Allele length
AssemblyAllele length
hg3810099
hg1910099
hg1810099
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsesv3423185, esv3331502
SamplesNA12878, NA12892
Known GenesKGFLP1
MethodSequencing
Analysis
PlatformIllumina
Comments
Reference1000_Genomes_Consortium_Pilot_Project
Pubmed ID20981092
Accession Number(s)dgv4373e59
Frequency
Sample Size185
Observed Gain2
Observed Loss0
Observed Complex0
Frequencyn/a


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