A curated catalogue of human genomic structural variation




Variant Details

Variant: dgv4549e59



Internal ID22765769
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr9:138261081..138262979hg38UCSC Ensembl
chr9:141151531..141153429hg19UCSC Ensembl
chr9:140271352..140273250hg18UCSC Ensembl
Cytoband9q34.3
Allele length
AssemblyAllele length
hg381899
hg191899
hg181899
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsesv3402119, esv3427616, esv3366268, esv3387447, esv3391242, esv3358408
SamplesNA12891, NA19238, NA19239, NA12878, NA12892, NA19240
Known Genes
MethodSequencing
Analysis
PlatformIllumina
Comments
Reference1000_Genomes_Consortium_Pilot_Project
Pubmed ID20981092
Accession Number(s)dgv4549e59
Frequency
Sample Size185
Observed Gain6
Observed Loss0
Observed Complex0
Frequencyn/a


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