A curated catalogue of human genomic structural variation




Variant Details

Variant: essv7840687



Internal ID13698957
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr9:76836357..76836358hg38UCSC Ensembl
Innerchr9:76836341..76836374hg38UCSC Ensembl
Outerchr9:76836340..76836375hg38UCSC Ensembl
chr9:79451273..79451274hg19UCSC Ensembl
Innerchr9:79451257..79451290hg19UCSC Ensembl
Outerchr9:79451256..79451291hg19UCSC Ensembl
chr9:78641093..78641094hg18UCSC Ensembl
Innerchr9:78641110..78641077hg18UCSC Ensembl
Outerchr9:78641076..78641111hg18UCSC Ensembl
Cytoband9q21.13
Allele length
AssemblyAllele length
hg38200
hg19200
hg18200
Variant TypeCNV mobile element insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsesv3308196
Supporting Variants
SamplesNA12891
Known GenesPRUNE2
MethodSequencing
Analysis
PlatformIllumina
Comments
Reference1000_Genomes_Consortium_Pilot_Project
Pubmed ID20981092
Accession Number(s)essv7840687
Frequency
Sample Size185
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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