A curated catalogue of human genomic structural variation




Variant Details

Variant: esv3388451



Internal ID15235418
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr15:53161413..53161425hg38UCSC Ensembl
Innerchr15:53161404..53161431hg38UCSC Ensembl
Outerchr15:53161392..53161446hg38UCSC Ensembl
chr15:53453610..53453622hg19UCSC Ensembl
Innerchr15:53453601..53453628hg19UCSC Ensembl
Outerchr15:53453589..53453643hg19UCSC Ensembl
chr15:51240902..51240914hg18UCSC Ensembl
Innerchr15:51240920..51240893hg18UCSC Ensembl
Outerchr15:51240881..51240935hg18UCSC Ensembl
Cytoband15q21.3
Allele length
AssemblyAllele length
hg38283
hg19283
hg18283
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsessv8968262, essv8968269, essv8968271, essv8968266, essv8968280, essv8968272, essv8968264, essv8968268, essv8968263, essv8968278, essv8968258, essv8968275, essv8968274, essv8968265, essv8968279, essv8968267, essv8968276, essv8968260, essv8968273, essv8968283, essv8968282, essv8968277, essv8968261
SamplesNA11830, NA18561, NA18870, NA18526, NA12750, NA07357, NA07346, NA18563, NA18582, NA18571, NA12003, NA11894, NA19225, NA12144, NA18909, NA19108, NA18952, NA19147, NA07051, NA07037, NA06986, NA19102, NA19129
Known Genes
MethodSequencing
Analysis
PlatformIllumina
Comments
Reference1000_Genomes_Consortium_Pilot_Project
Pubmed ID20981092
Accession Number(s)esv3388451
Frequency
Sample Size185
Observed Gain23
Observed Loss0
Observed Complex0
Frequencyn/a


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