A curated catalogue of human genomic structural variation




Variant Details

Variant: dgv4393e59



Internal ID22765613
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr9:63108960..63132358hg38UCSC Ensembl
chr9:67013932..67037330hg19UCSC Ensembl
chr9:66753752..66777150hg18UCSC Ensembl
Cytoband9q12
Allele length
AssemblyAllele length
hg3823399
hg1923399
hg1823399
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsesv3328902, esv3448720, esv3451680
SamplesNA19239, NA12878, NA12892
Known GenesLOC286297
MethodSequencing
Analysis
PlatformIllumina
Comments
Reference1000_Genomes_Consortium_Pilot_Project
Pubmed ID20981092
Accession Number(s)dgv4393e59
Frequency
Sample Size185
Observed Gain3
Observed Loss0
Observed Complex0
Frequencyn/a


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