A curated catalogue of human genomic structural variation




Variant Details

Variant: dgv4532e59



Internal ID22765752
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr9:133382386..133383862hg38UCSC Ensembl
chr9:136249258..136249646hg19UCSC Ensembl
chr9:135239079..135239467hg18UCSC Ensembl
Cytoband9q34.2
Allele length
AssemblyAllele length
hg381477
hg19389
hg18389
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsesv3355251, esv3361911
SamplesNA12878, NA19240
Known GenesC9orf96
MethodSequencing
Analysis
Platform454
SOLiD
Comments
Reference1000_Genomes_Consortium_Pilot_Project
Pubmed ID20981092
Accession Number(s)dgv4532e59
Frequency
Sample Size185
Observed Gain2
Observed Loss0
Observed Complex0
Frequencyn/a


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