A curated catalogue of human genomic structural variation




Variant Details

Variant: esv3446582



Internal ID15293532
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr9:65676015..65688113hg38UCSC Ensembl
Innerchr9:65677015..65687113hg38UCSC Ensembl
Outerchr9:65675015..65689113hg38UCSC Ensembl
chr9:70477932..70490030hg19UCSC Ensembl
Innerchr9:70478932..70489030hg19UCSC Ensembl
Outerchr9:70476932..70491030hg19UCSC Ensembl
chr9:69717752..69729850hg18UCSC Ensembl
Innerchr9:69718752..69728850hg18UCSC Ensembl
Outerchr9:69716752..69730850hg18UCSC Ensembl
Cytoband9q12
Allele length
AssemblyAllele length
hg3812099
hg1912099
hg1812099
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsessv8697325
SamplesNA12878
Known GenesCBWD3, CBWD5
MethodSequencing
Analysis
PlatformIllumina
Comments
Reference1000_Genomes_Consortium_Pilot_Project
Pubmed ID20981092
Accession Number(s)esv3446582
Frequency
Sample Size185
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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