A curated catalogue of human genomic structural variation




Variant Details

Variant: dgv4406e59



Internal ID22765626
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr9:63848598..63902496hg38UCSC Ensembl
chr9:68444332..68498230hg19UCSC Ensembl
chr9:67934152..67988050hg18UCSC Ensembl
Cytoband9q12
Allele length
AssemblyAllele length
hg3853899
hg1953899
hg1853899
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsesv3419053, esv3446385, esv3440281, esv3402601, esv3429288, esv3441343
SamplesNA12891, NA19238, NA19239, NA12878, NA12892, NA19240
Known GenesLOC642236
MethodSequencing
Analysis
PlatformIllumina
Comments
Reference1000_Genomes_Consortium_Pilot_Project
Pubmed ID20981092
Accession Number(s)dgv4406e59
Frequency
Sample Size185
Observed Gain6
Observed Loss0
Observed Complex0
Frequencyn/a


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