A curated catalogue of human genomic structural variation




Variant Details

Variant: esv3363452



Internal ID15210430
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr9:62477855..62486353hg38UCSC Ensembl
Innerchr9:62478855..62485353hg38UCSC Ensembl
Outerchr9:62476855..62487353hg38UCSC Ensembl
chr9:46789156..46797654hg19UCSC Ensembl
Innerchr9:46790156..46796654hg19UCSC Ensembl
Outerchr9:46788156..46798654hg19UCSC Ensembl
chr9:46629152..46637650hg18UCSC Ensembl
Innerchr9:46630152..46636650hg18UCSC Ensembl
Outerchr9:46628152..46638650hg18UCSC Ensembl
Cytoband9p11.2
Allele length
AssemblyAllele length
hg388499
hg198499
hg188499
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv4376e59
Supporting Variantsessv8696987
SamplesNA12892
Known Genes
MethodSequencing
Analysis
PlatformIllumina
Comments
Reference1000_Genomes_Consortium_Pilot_Project
Pubmed ID20981092
Accession Number(s)esv3363452
Frequency
Sample Size185
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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