A curated catalogue of human genomic structural variation




Variant Details

Variant: esv3336164



Internal ID14836435
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr9:17274290..17274339hg38UCSC Ensembl
Innerchr9:17274302..17274327hg38UCSC Ensembl
Outerchr9:17274253..17274376hg38UCSC Ensembl
chr9:17274288..17274337hg19UCSC Ensembl
Innerchr9:17274300..17274325hg19UCSC Ensembl
Outerchr9:17274251..17274374hg19UCSC Ensembl
chr9:17264288..17264337hg18UCSC Ensembl
Innerchr9:17264325..17264300hg18UCSC Ensembl
Outerchr9:17264251..17264374hg18UCSC Ensembl
Cytoband9p22.2
Allele length
AssemblyAllele length
hg38179
hg19179
hg18179
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsessv8943861, essv8943863, essv8943862
SamplesNA18501, NA18856, NA18519
Known GenesCNTLN
MethodSequencing
Analysis
PlatformIllumina
Comments
Reference1000_Genomes_Consortium_Pilot_Project
Pubmed ID20981092
Accession Number(s)esv3336164
Frequency
Sample Size185
Observed Gain3
Observed Loss0
Observed Complex0
Frequencyn/a


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