A curated catalogue of human genomic structural variation




Variant Details

Variant: essv7865519



Internal ID13317890
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr11:109263840..109263852hg38UCSC Ensembl
Innerchr11:109263842..109263850hg38UCSC Ensembl
Outerchr11:109263838..109263854hg38UCSC Ensembl
chr11:109134567..109134579hg19UCSC Ensembl
Innerchr11:109134569..109134577hg19UCSC Ensembl
Outerchr11:109134565..109134581hg19UCSC Ensembl
chr11:108639777..108639789hg18UCSC Ensembl
Innerchr11:108639779..108639787hg18UCSC Ensembl
Outerchr11:108639775..108639791hg18UCSC Ensembl
Cytoband11q22.3
Allele length
AssemblyAllele length
hg3851
hg1951
hg1851
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsesv3360163
Supporting Variants
SamplesNA12005
Known Genes
MethodSequencing
Analysis
PlatformIllumina
Comments
Reference1000_Genomes_Consortium_Pilot_Project
Pubmed ID20981092
Accession Number(s)essv7865519
Frequency
Sample Size185
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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