A curated catalogue of human genomic structural variation




Variant Details

Variant: essv7732563



Internal ID14851783
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr10:87622434..87622444hg38UCSC Ensembl
Outerchr10:87622234..87622644hg38UCSC Ensembl
Innerchr10:89382191..89382201hg19UCSC Ensembl
Outerchr10:89381991..89382401hg19UCSC Ensembl
Innerchr10:89372171..89372181hg18UCSC Ensembl
Outerchr10:89371971..89372381hg18UCSC Ensembl
Cytoband10q23.2
Allele length
AssemblyAllele length
hg38411
hg19411
hg18411
Variant TypeCNV tandem duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsesv3302713
Supporting Variants
SamplesNA19108
Known Genes
MethodSequencing
Analysis
PlatformIllumina
Comments
Reference1000_Genomes_Consortium_Pilot_Project
Pubmed ID20981092
Accession Number(s)essv7732563
Frequency
Sample Size185
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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