A curated catalogue of human genomic structural variation




Variant Details

Variant: esv3434793



Internal ID15281747
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr13:110873604..110874502hg38UCSC Ensembl
Innerchr13:110873603..110874503hg38UCSC Ensembl
Outerchr13:110872604..110875502hg38UCSC Ensembl
chr13:111525951..111526849hg19UCSC Ensembl
Innerchr13:111525950..111526850hg19UCSC Ensembl
Outerchr13:111524951..111527849hg19UCSC Ensembl
chr13:110323952..110324850hg18UCSC Ensembl
Innerchr13:110324851..110323951hg18UCSC Ensembl
Outerchr13:110322952..110325850hg18UCSC Ensembl
Cytoband13q34
Allele length
AssemblyAllele length
hg38899
hg19899
hg18899
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv1114e59
Supporting Variantsessv8688758
SamplesNA19240
Known Genes
MethodSequencing
Analysis
PlatformIllumina
Comments
Reference1000_Genomes_Consortium_Pilot_Project
Pubmed ID20981092
Accession Number(s)esv3434793
Frequency
Sample Size185
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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