A curated catalogue of human genomic structural variation




Variant Details

Variant: dgv4370e59



Internal ID22765590
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr9:62350755..62353553hg38UCSC Ensembl
chr9:46662056..46664854hg19UCSC Ensembl
chr9:46502052..46504850hg18UCSC Ensembl
Cytoband9p11.2
Allele length
AssemblyAllele length
hg382799
hg192799
hg182799
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsesv3394344, esv3448488, esv3415786
SamplesNA19239, NA12878, NA12892
Known Genes
MethodSequencing
Analysis
PlatformIllumina
Comments
Reference1000_Genomes_Consortium_Pilot_Project
Pubmed ID20981092
Accession Number(s)dgv4370e59
Frequency
Sample Size185
Observed Gain3
Observed Loss0
Observed Complex0
Frequencyn/a


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