A curated catalogue of human genomic structural variation




Variant Details

Variant: esv3382906



Internal ID14883182
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr11:6449546..6450544hg38UCSC Ensembl
Innerchr11:6449545..6450545hg38UCSC Ensembl
Outerchr11:6448546..6451544hg38UCSC Ensembl
chr11:6470776..6471774hg19UCSC Ensembl
Innerchr11:6470775..6471775hg19UCSC Ensembl
Outerchr11:6469776..6472774hg19UCSC Ensembl
chr11:6427352..6428350hg18UCSC Ensembl
Innerchr11:6428351..6427351hg18UCSC Ensembl
Outerchr11:6426352..6429350hg18UCSC Ensembl
Cytoband11p15.4
Allele length
AssemblyAllele length
hg38999
hg19999
hg18999
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsessv8688485
SamplesNA19239
Known GenesTRIM3
MethodSequencing
Analysis
PlatformIllumina
Comments
Reference1000_Genomes_Consortium_Pilot_Project
Pubmed ID20981092
Accession Number(s)esv3382906
Frequency
Sample Size185
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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