A curated catalogue of human genomic structural variation




Variant Details

Variant: esv3352534



Internal ID15199515
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr11:64379404..64380702hg38UCSC Ensembl
Innerchr11:64379702..64380404hg38UCSC Ensembl
Outerchr11:64378404..64381702hg38UCSC Ensembl
chr11:64146876..64148174hg19UCSC Ensembl
Innerchr11:64147174..64147876hg19UCSC Ensembl
Outerchr11:64145876..64149174hg19UCSC Ensembl
chr11:63903452..63904750hg18UCSC Ensembl
Innerchr11:63904452..63903750hg18UCSC Ensembl
Outerchr11:63902452..63905750hg18UCSC Ensembl
Cytoband11q13.1
Allele length
AssemblyAllele length
hg381299
hg191299
hg181299
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsessv8688482
SamplesNA19240
Known Genes
MethodSequencing
Analysis
PlatformIllumina
Comments
Reference1000_Genomes_Consortium_Pilot_Project
Pubmed ID20981092
Accession Number(s)esv3352534
Frequency
Sample Size185
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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