A curated catalogue of human genomic structural variation




Variant Details

Variant: essv7838265



Internal ID13698115
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr11:81572822..81572823hg38UCSC Ensembl
Innerchr11:81572787..81572858hg38UCSC Ensembl
Outerchr11:81572786..81572859hg38UCSC Ensembl
chr11:81283864..81283865hg19UCSC Ensembl
Innerchr11:81283829..81283900hg19UCSC Ensembl
Outerchr11:81283828..81283901hg19UCSC Ensembl
chr11:80961512..80961513hg18UCSC Ensembl
Innerchr11:80961548..80961477hg18UCSC Ensembl
Outerchr11:80961476..80961549hg18UCSC Ensembl
Cytoband11q14.1
Allele length
AssemblyAllele length
hg38307
hg19307
hg18307
Variant TypeCNV mobile element insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsesv3308425
Supporting Variants
SamplesNA12891
Known Genes
MethodSequencing
Analysis
PlatformIllumina
Comments
Reference1000_Genomes_Consortium_Pilot_Project
Pubmed ID20981092
Accession Number(s)essv7838265
Frequency
Sample Size185
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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