A curated catalogue of human genomic structural variation




Variant Details

Variant: esv3346481



Internal ID15193463
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr11:92705296..92706130hg38UCSC Ensembl
Innerchr11:92705296..92706130hg38UCSC Ensembl
Outerchr11:92704755..92706464hg38UCSC Ensembl
chr11:92438462..92439296hg19UCSC Ensembl
Innerchr11:92438462..92439296hg19UCSC Ensembl
Outerchr11:92437921..92439630hg19UCSC Ensembl
chr11:92078110..92078944hg18UCSC Ensembl
Innerchr11:92078110..92078944hg18UCSC Ensembl
Outerchr11:92077569..92079278hg18UCSC Ensembl
Cytoband11q14.3
Allele length
AssemblyAllele length
hg38835
hg19835
hg18835
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsessv8651830
SamplesNA19240
Known GenesFAT3
MethodSequencing
Analysis
PlatformSOLiD
Comments
Reference1000_Genomes_Consortium_Pilot_Project
Pubmed ID20981092
Accession Number(s)esv3346481
Frequency
Sample Size185
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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