A curated catalogue of human genomic structural variation




Variant Details

Variant: dgv4376e59



Internal ID22765596
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr9:62477855..62489053hg38UCSC Ensembl
chr9:46789156..46800354hg19UCSC Ensembl
chr9:46629152..46640350hg18UCSC Ensembl
Cytoband9p11.2
Allele length
AssemblyAllele length
hg3811199
hg1911199
hg1811199
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsesv3347872, esv3363452
SamplesNA12878, NA12892
Known Genes
MethodSequencing
Analysis
PlatformIllumina
Comments
Reference1000_Genomes_Consortium_Pilot_Project
Pubmed ID20981092
Accession Number(s)dgv4376e59
Frequency
Sample Size185
Observed Gain2
Observed Loss0
Observed Complex0
Frequencyn/a


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