A curated catalogue of human genomic structural variation




Variant Details

Variant: dgv4465e59



Internal ID20131214
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr9:86052484..86054115hg38UCSC Ensembl
chr9:88667399..88669030hg19UCSC Ensembl
chr9:87857219..87858850hg18UCSC Ensembl
Cytoband9q21.33
Allele length
AssemblyAllele length
hg381632
hg191632
hg181632
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsesv3451863, esv3450099
SamplesNA19240
Known GenesGOLM1
MethodSequencing
Analysis
PlatformIllumina
SOLiD
Comments
Reference1000_Genomes_Consortium_Pilot_Project
Pubmed ID20981092
Accession Number(s)dgv4465e59
Frequency
Sample Size185
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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