A curated catalogue of human genomic structural variation




Variant Details

Variant: essv8672059



Internal ID15029355
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 StatusS
Merged Variantsesv3399724
Supporting Variants
SamplesNA19238
Known Genes
MethodSequencing
Analysis
PlatformIllumina
Comments
Reference1000_Genomes_Consortium_Pilot_Project
Pubmed ID20981092
Accession Number(s)essv8672059
Frequency
Sample Size185
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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