A curated catalogue of human genomic structural variation




Variant Details

Variant: essv8640134



Internal ID14798776
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr11:10802030..10802030hg38UCSC Ensembl
Innerchr11:10802029..10802031hg38UCSC Ensembl
Outerchr11:10801990..10802050hg38UCSC Ensembl
chr11:10823577..10823577hg19UCSC Ensembl
Innerchr11:10823576..10823578hg19UCSC Ensembl
Outerchr11:10823537..10823597hg19UCSC Ensembl
chr11:10780153..10780153hg18UCSC Ensembl
Innerchr11:10780154..10780152hg18UCSC Ensembl
Outerchr11:10780113..10780173hg18UCSC Ensembl
Cytoband11p15.3
Allele length
AssemblyAllele length
hg3879
hg1979
hg1879
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsesv3362770
Supporting Variants
Samples
Known GenesEIF4G2
MethodSequencing
Analysis
Platform454
Comments
Reference1000_Genomes_Consortium_Pilot_Project
Pubmed ID20981092
Accession Number(s)essv8640134
Frequency
Sample Size185
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


Hosted by The Centre for Applied Genomics
Grant support for DGV
Please read the usage disclaimer