A curated catalogue of human genomic structural variation




Variant Details

Variant: esv3355802



Internal ID15202783
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr11:43335381..43335403hg38UCSC Ensembl
Innerchr11:43335385..43335397hg38UCSC Ensembl
Outerchr11:43335365..43335419hg38UCSC Ensembl
chr11:43356931..43356953hg19UCSC Ensembl
Innerchr11:43356935..43356947hg19UCSC Ensembl
Outerchr11:43356915..43356969hg19UCSC Ensembl
chr11:43313507..43313529hg18UCSC Ensembl
Innerchr11:43313523..43313511hg18UCSC Ensembl
Outerchr11:43313491..43313545hg18UCSC Ensembl
Cytoband11p12
Allele length
AssemblyAllele length
hg38166
hg19166
hg18166
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsessv8952913, essv8952919, essv8952918, essv8952914, essv8952917, essv8952920, essv8952916
SamplesNA11829, NA11931, NA11918, NA11919, NA11881, NA12763, NA12006
Known GenesAPI5
MethodSequencing
Analysis
PlatformIllumina
Comments
Reference1000_Genomes_Consortium_Pilot_Project
Pubmed ID20981092
Accession Number(s)esv3355802
Frequency
Sample Size185
Observed Gain7
Observed Loss0
Observed Complex0
Frequencyn/a


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