A curated catalogue of human genomic structural variation




Variant Details

Variant: esv3418790



Internal ID15265748
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr9:65807615..65815013hg38UCSC Ensembl
Innerchr9:65808615..65814013hg38UCSC Ensembl
Outerchr9:65806615..65816013hg38UCSC Ensembl
chr9:70351032..70358430hg19UCSC Ensembl
Innerchr9:70352032..70357430hg19UCSC Ensembl
Outerchr9:70350032..70359430hg19UCSC Ensembl
chr9:69590852..69598250hg18UCSC Ensembl
Innerchr9:69591852..69597250hg18UCSC Ensembl
Outerchr9:69589852..69599250hg18UCSC Ensembl
Cytoband9q12
Allele length
AssemblyAllele length
hg387399
hg197399
hg187399
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsessv8697310
SamplesNA12892
Known Genes
MethodSequencing
Analysis
PlatformIllumina
Comments
Reference1000_Genomes_Consortium_Pilot_Project
Pubmed ID20981092
Accession Number(s)esv3418790
Frequency
Sample Size185
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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