A curated catalogue of human genomic structural variation




Variant Details

Variant: esv3369183



Internal ID15216159
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr11:15876003..15876017hg38UCSC Ensembl
Innerchr11:15876005..15876015hg38UCSC Ensembl
Outerchr11:15875991..15876029hg38UCSC Ensembl
chr11:15897549..15897563hg19UCSC Ensembl
Innerchr11:15897551..15897561hg19UCSC Ensembl
Outerchr11:15897537..15897575hg19UCSC Ensembl
chr11:15854125..15854139hg18UCSC Ensembl
Innerchr11:15854137..15854127hg18UCSC Ensembl
Outerchr11:15854113..15854151hg18UCSC Ensembl
Cytoband11p15.2
Allele length
AssemblyAllele length
hg3854
hg1954
hg1854
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsessv7865446
SamplesNA12005
Known Genes
MethodSequencing
Analysis
PlatformIllumina
Comments
Reference1000_Genomes_Consortium_Pilot_Project
Pubmed ID20981092
Accession Number(s)esv3369183
Frequency
Sample Size185
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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