A curated catalogue of human genomic structural variation




Variant Details

Variant: esv3360510



Internal ID15207489
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr13:26376207..26376237hg38UCSC Ensembl
Innerchr13:26376202..26376239hg38UCSC Ensembl
Outerchr13:26376172..26376269hg38UCSC Ensembl
chr13:26950344..26950374hg19UCSC Ensembl
Innerchr13:26950339..26950376hg19UCSC Ensembl
Outerchr13:26950309..26950406hg19UCSC Ensembl
chr13:25848344..25848374hg18UCSC Ensembl
Innerchr13:25848376..25848339hg18UCSC Ensembl
Outerchr13:25848309..25848406hg18UCSC Ensembl
Cytoband13q12.13
Allele length
AssemblyAllele length
hg38242
hg19242
hg18242
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsessv8959429, essv8959432, essv8959430, essv8959427, essv8959431, essv8959428
SamplesNA18861, NA18489, NA18516, NA18499, NA18858, NA19093
Known GenesCDK8
MethodSequencing
Analysis
PlatformIllumina
Comments
Reference1000_Genomes_Consortium_Pilot_Project
Pubmed ID20981092
Accession Number(s)esv3360510
Frequency
Sample Size185
Observed Gain6
Observed Loss0
Observed Complex0
Frequencyn/a


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