A curated catalogue of human genomic structural variation




Variant Details

Variant: dgv4531e59



Internal ID20131280
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr9:132376744..132379142hg38UCSC Ensembl
chr9:135252131..135254529hg19UCSC Ensembl
chr9:134241952..134244350hg18UCSC Ensembl
Cytoband9q34.13
Allele length
AssemblyAllele length
hg382399
hg192399
hg182399
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsesv3407895, esv3382808
SamplesNA19239, NA19240
Known GenesTTF1
MethodSequencing
Analysis
PlatformIllumina
Comments
Reference1000_Genomes_Consortium_Pilot_Project
Pubmed ID20981092
Accession Number(s)dgv4531e59
Frequency
Sample Size185
Observed Gain2
Observed Loss0
Observed Complex0
Frequencyn/a


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