A curated catalogue of human genomic structural variation




Variant Details

Variant: esv3437892



Internal ID15284845
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr11:69278609..69280207hg38UCSC Ensembl
Innerchr11:69279207..69279609hg38UCSC Ensembl
Outerchr11:69277609..69281207hg38UCSC Ensembl
chr11:69046076..69047674hg19UCSC Ensembl
Innerchr11:69046674..69047076hg19UCSC Ensembl
Outerchr11:69045076..69048674hg19UCSC Ensembl
chr11:68802652..68804250hg18UCSC Ensembl
Innerchr11:68803652..68803250hg18UCSC Ensembl
Outerchr11:68801652..68805250hg18UCSC Ensembl
Cytoband11q13.2
Allele length
AssemblyAllele length
hg381599
hg191599
hg181599
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsessv8688501
SamplesNA19240
Known Genes
MethodSequencing
Analysis
PlatformIllumina
Comments
Reference1000_Genomes_Consortium_Pilot_Project
Pubmed ID20981092
Accession Number(s)esv3437892
Frequency
Sample Size185
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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