A curated catalogue of human genomic structural variation




Variant Details

Variant: dgv4372e59



Internal ID22765592
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr9:62393655..62408453hg38UCSC Ensembl
chr9:46704956..46719754hg19UCSC Ensembl
chr9:46544952..46559750hg18UCSC Ensembl
Cytoband9p11.2
Allele length
AssemblyAllele length
hg3814799
hg1914799
hg1814799
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsesv3435595, esv3443294
SamplesNA12878, NA12892
Known GenesKGFLP1
MethodSequencing
Analysis
PlatformIllumina
Comments
Reference1000_Genomes_Consortium_Pilot_Project
Pubmed ID20981092
Accession Number(s)dgv4372e59
Frequency
Sample Size185
Observed Gain2
Observed Loss0
Observed Complex0
Frequencyn/a


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