A curated catalogue of human genomic structural variation




Variant Details

Variant: esv3399724



Internal ID15246687
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr11:27003666..27003727hg38UCSC Ensembl
Innerchr11:27003653..27003740hg38UCSC Ensembl
Outerchr11:27003592..27003801hg38UCSC Ensembl
chr11:27025213..27025274hg19UCSC Ensembl
Innerchr11:27025200..27025287hg19UCSC Ensembl
Outerchr11:27025139..27025348hg19UCSC Ensembl
chr11:26981789..26981850hg18UCSC Ensembl
Innerchr11:26981863..26981776hg18UCSC Ensembl
Outerchr11:26981715..26981924hg18UCSC Ensembl
Cytoband11p14.2
Allele length
AssemblyAllele length
hg38105
hg19105
hg18105
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsessv8672060, essv8672058, essv8672059
SamplesNA19238, NA19239, NA19240
Known Genes
MethodSequencing
Analysis
PlatformIllumina
Comments
Reference1000_Genomes_Consortium_Pilot_Project
Pubmed ID20981092
Accession Number(s)esv3399724
Frequency
Sample Size185
Observed Gain3
Observed Loss0
Observed Complex0
Frequencyn/a


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