A curated catalogue of human genomic structural variation




Variant Details

Variant: esv3309832



Internal ID15156783
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr11:27003638..27003639hg38UCSC Ensembl
Innerchr11:27003528..27003749hg38UCSC Ensembl
Outerchr11:27003527..27003750hg38UCSC Ensembl
chr11:27025185..27025186hg19UCSC Ensembl
Innerchr11:27025075..27025296hg19UCSC Ensembl
Outerchr11:27025074..27025297hg19UCSC Ensembl
chr11:26981761..26981762hg18UCSC Ensembl
Innerchr11:26981872..26981651hg18UCSC Ensembl
Outerchr11:26981650..26981873hg18UCSC Ensembl
Cytoband11p14.2
Allele length
AssemblyAllele length
hg38105
hg19105
hg18105
Variant TypeCNV mobile element insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsessv7836791
SamplesNA19239
Known Genes
MethodSequencing
Analysis
PlatformIllumina
Comments
Reference1000_Genomes_Consortium_Pilot_Project
Pubmed ID20981092
Accession Number(s)esv3309832
Frequency
Sample Size185
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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