A curated catalogue of human genomic structural variation




Variant Details

Variant: esv3302713



Internal ID15149661
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr10:87622333..87622544hg38UCSC Ensembl
Innerchr10:87622433..87622444hg38UCSC Ensembl
Outerchr10:87622233..87622644hg38UCSC Ensembl
chr10:89382090..89382301hg19UCSC Ensembl
Innerchr10:89382190..89382201hg19UCSC Ensembl
Outerchr10:89381990..89382401hg19UCSC Ensembl
chr10:89372070..89372281hg18UCSC Ensembl
Innerchr10:89372170..89372181hg18UCSC Ensembl
Outerchr10:89371970..89372381hg18UCSC Ensembl
Cytoband10q23.2
Allele length
AssemblyAllele length
hg38212
hg19212
hg18212
Variant TypeCNV tandem duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsessv7732563
SamplesNA19108
Known Genes
MethodSequencing
Analysis
PlatformIllumina
Comments
Reference1000_Genomes_Consortium_Pilot_Project
Pubmed ID20981092
Accession Number(s)esv3302713
Frequency
Sample Size185
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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