A curated catalogue of human genomic structural variation




Variant Details

Variant: essv8688277



Internal ID13693094
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr11:3653646..3655044hg38UCSC Ensembl
Innerchr11:3654044..3654646hg38UCSC Ensembl
Outerchr11:3652646..3656044hg38UCSC Ensembl
chr11:3674876..3676274hg19UCSC Ensembl
Innerchr11:3675274..3675876hg19UCSC Ensembl
Outerchr11:3673876..3677274hg19UCSC Ensembl
chr11:3631452..3632850hg18UCSC Ensembl
Innerchr11:3632452..3631850hg18UCSC Ensembl
Outerchr11:3630452..3633850hg18UCSC Ensembl
Cytoband11p15.4
Allele length
AssemblyAllele length
hg381399
hg191399
hg181399
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag1
Merged StatusS
Merged Variantsesv3446921
Supporting Variants
SamplesNA12891
Known GenesART1
MethodSequencing
Analysis
PlatformIllumina
Comments
Reference1000_Genomes_Consortium_Pilot_Project
Pubmed ID20981092
Accession Number(s)essv8688277
Frequency
Sample Size185
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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