A curated catalogue of human genomic structural variation




Variant Details

Variant: esv3361899



Internal ID14862160
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr11:67367105..67370103hg38UCSC Ensembl
Innerchr11:67368105..67369103hg38UCSC Ensembl
Outerchr11:67366105..67371103hg38UCSC Ensembl
chr11:67134576..67137574hg19UCSC Ensembl
Innerchr11:67135576..67136574hg19UCSC Ensembl
Outerchr11:67133576..67138574hg19UCSC Ensembl
chr11:66891152..66894150hg18UCSC Ensembl
Innerchr11:66892152..66893150hg18UCSC Ensembl
Outerchr11:66890152..66895150hg18UCSC Ensembl
Cytoband11q13.1
Allele length
AssemblyAllele length
hg382999
hg192999
hg182999
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsessv8688494
SamplesNA19239
Known GenesCLCF1, LOC100130987
MethodSequencing
Analysis
PlatformIllumina
Comments
Reference1000_Genomes_Consortium_Pilot_Project
Pubmed ID20981092
Accession Number(s)esv3361899
Frequency
Sample Size185
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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