A curated catalogue of human genomic structural variation




Variant Details

Variant: dgv4351e59



Internal ID22765571
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr9:64457457..64470879hg38UCSC Ensembl
chr9:43026056..43039454hg19UCSC Ensembl
chr9:43016052..43029450hg18UCSC Ensembl
Cytoband9p11.2
Allele length
AssemblyAllele length
hg3813423
hg1913399
hg1813399
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsesv3353453, esv3332978
SamplesNA19239, NA12892
Known GenesFAM95B1
MethodSequencing
Analysis
PlatformIllumina
Comments
Reference1000_Genomes_Consortium_Pilot_Project
Pubmed ID20981092
Accession Number(s)dgv4351e59
Frequency
Sample Size185
Observed Gain2
Observed Loss0
Observed Complex0
Frequencyn/a


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