A curated catalogue of human genomic structural variation




Variant Details

Variant: essv7755743



Internal ID13195503
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr11:43335387..43335388hg38UCSC Ensembl
Innerchr11:43335356..43335419hg38UCSC Ensembl
Outerchr11:43335355..43335420hg38UCSC Ensembl
chr11:43356937..43356938hg19UCSC Ensembl
Innerchr11:43356906..43356969hg19UCSC Ensembl
Outerchr11:43356905..43356970hg19UCSC Ensembl
chr11:43313513..43313514hg18UCSC Ensembl
Innerchr11:43313545..43313482hg18UCSC Ensembl
Outerchr11:43313481..43313546hg18UCSC Ensembl
Cytoband11p12
Allele length
AssemblyAllele length
hg38166
hg19166
hg18166
Variant TypeCNV mobile element insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsesv3306211
Supporting Variants
SamplesNA11918
Known GenesAPI5
MethodSequencing
Analysis
PlatformIllumina
Comments
Reference1000_Genomes_Consortium_Pilot_Project
Pubmed ID20981092
Accession Number(s)essv7755743
Frequency
Sample Size185
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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