A curated catalogue of human genomic structural variation




Variant Details

Variant: esv3307869



Internal ID15154817
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr11:101041049..101041050hg38UCSC Ensembl
Innerchr11:101041032..101041067hg38UCSC Ensembl
Outerchr11:101041031..101041068hg38UCSC Ensembl
chr11:100911780..100911781hg19UCSC Ensembl
Innerchr11:100911763..100911798hg19UCSC Ensembl
Outerchr11:100911762..100911799hg19UCSC Ensembl
chr11:100416990..100416991hg18UCSC Ensembl
Innerchr11:100417008..100416973hg18UCSC Ensembl
Outerchr11:100416972..100417009hg18UCSC Ensembl
Cytoband11q22.1
Allele length
AssemblyAllele length
hg38293
hg19293
hg18293
Variant TypeCNV mobile element insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsessv7824865, essv7771092, essv7804933, essv7817482, essv7782724, essv7773636, essv7792807, essv7784066, essv7801673, essv7800296, essv7795695, essv7790715, essv7809651, essv7788704, essv7813983, essv7777422
SamplesNA11995, NA11931, NA12750, NA12155, NA18563, NA11918, NA07347, NA12872, NA11919, NA12716, NA11881, NA12873, NA12874, NA06986, NA12006, NA07000
Known GenesPGR
MethodSequencing
Analysis
PlatformRoche 454
Comments
Reference1000_Genomes_Consortium_Pilot_Project
Pubmed ID20981092
Accession Number(s)esv3307869
Frequency
Sample Size185
Observed Gain16
Observed Loss0
Observed Complex0
Frequencyn/a


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