A curated catalogue of human genomic structural variation




Variant Details

Variant: esv3364981



Internal ID15211958
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr11:58050604..58053502hg38UCSC Ensembl
Innerchr11:58051604..58052502hg38UCSC Ensembl
Outerchr11:58049604..58054502hg38UCSC Ensembl
chr11:57818076..57820974hg19UCSC Ensembl
Innerchr11:57819076..57819974hg19UCSC Ensembl
Outerchr11:57817076..57821974hg19UCSC Ensembl
chr11:57574652..57577550hg18UCSC Ensembl
Innerchr11:57575652..57576550hg18UCSC Ensembl
Outerchr11:57573652..57578550hg18UCSC Ensembl
Cytoband11q12.1
Allele length
AssemblyAllele length
hg382899
hg192899
hg182899
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsessv8688457
SamplesNA12891
Known GenesOR9Q1
MethodSequencing
Analysis
PlatformIllumina
Comments
Reference1000_Genomes_Consortium_Pilot_Project
Pubmed ID20981092
Accession Number(s)esv3364981
Frequency
Sample Size185
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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