A curated catalogue of human genomic structural variation




Variant Details

Variant: esv3441171



Internal ID15288124
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr9:76931383..76931400hg38UCSC Ensembl
Innerchr9:76931354..76931429hg38UCSC Ensembl
Outerchr9:76931337..76931446hg38UCSC Ensembl
chr9:79546299..79546316hg19UCSC Ensembl
Innerchr9:79546270..79546345hg19UCSC Ensembl
Outerchr9:79546253..79546362hg19UCSC Ensembl
chr9:78736119..78736136hg18UCSC Ensembl
Innerchr9:78736165..78736090hg18UCSC Ensembl
Outerchr9:78736073..78736182hg18UCSC Ensembl
Cytoband9q21.13
Allele length
AssemblyAllele length
hg3858
hg1958
hg1858
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsessv7864935
SamplesNA12005
Known Genes
MethodSequencing
Analysis
PlatformIllumina
Comments
Reference1000_Genomes_Consortium_Pilot_Project
Pubmed ID20981092
Accession Number(s)esv3441171
Frequency
Sample Size185
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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