A curated catalogue of human genomic structural variation




Variant Details

Variant: dgv4479e59



Internal ID20131228
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr9:90840749..90842947hg38UCSC Ensembl
chr9:93603031..93605229hg19UCSC Ensembl
chr9:92642852..92645050hg18UCSC Ensembl
Cytoband9q22.2
Allele length
AssemblyAllele length
hg382199
hg192199
hg182199
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsesv3392644, esv3433405, esv3411483
SamplesNA19239, NA19238, NA19240
Known GenesSYK
MethodSequencing
Analysis
PlatformIllumina
Comments
Reference1000_Genomes_Consortium_Pilot_Project
Pubmed ID20981092
Accession Number(s)dgv4479e59
Frequency
Sample Size185
Observed Gain3
Observed Loss0
Observed Complex0
Frequencyn/a


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