A curated catalogue of human genomic structural variation




Variant Details

Variant: dgv4394e59



Internal ID22765614
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr9:63132960..63145558hg38UCSC Ensembl
chr9:67037932..67050530hg19UCSC Ensembl
chr9:66777752..66790350hg18UCSC Ensembl
Cytoband9q12
Allele length
AssemblyAllele length
hg3812599
hg1912599
hg1812599
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsesv3344521, esv3379630
SamplesNA12878, NA12892
Known Genes
MethodSequencing
Analysis
PlatformIllumina
Comments
Reference1000_Genomes_Consortium_Pilot_Project
Pubmed ID20981092
Accession Number(s)dgv4394e59
Frequency
Sample Size185
Observed Gain2
Observed Loss0
Observed Complex0
Frequencyn/a


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