A curated catalogue of human genomic structural variation




Variant Details

Variant: essv8688275



Internal ID15010733
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr11:3653646..3654944hg38UCSC Ensembl
Innerchr11:3653944..3654646hg38UCSC Ensembl
Outerchr11:3652646..3655944hg38UCSC Ensembl
chr11:3674876..3676174hg19UCSC Ensembl
Innerchr11:3675174..3675876hg19UCSC Ensembl
Outerchr11:3673876..3677174hg19UCSC Ensembl
chr11:3631452..3632750hg18UCSC Ensembl
Innerchr11:3632452..3631750hg18UCSC Ensembl
Outerchr11:3630452..3633750hg18UCSC Ensembl
Cytoband11p15.4
Allele length
AssemblyAllele length
hg381299
hg191299
hg181299
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsesv3362096
Supporting Variants
SamplesNA19238
Known GenesART1
MethodSequencing
Analysis
PlatformIllumina
Comments
Reference1000_Genomes_Consortium_Pilot_Project
Pubmed ID20981092
Accession Number(s)essv8688275
Frequency
Sample Size185
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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