A curated catalogue of human genomic structural variation




Variant Details

Variant: esv3350972



Internal ID15197953
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr11:66597912..66598102hg38UCSC Ensembl
Innerchr11:66597911..66598103hg38UCSC Ensembl
Outerchr11:66597802..66598222hg38UCSC Ensembl
chr11:66365383..66365573hg19UCSC Ensembl
Innerchr11:66365382..66365574hg19UCSC Ensembl
Outerchr11:66365273..66365693hg19UCSC Ensembl
chr11:66121959..66122149hg18UCSC Ensembl
Innerchr11:66122150..66121958hg18UCSC Ensembl
Outerchr11:66121849..66122269hg18UCSC Ensembl
Cytoband11q13.1
Allele length
AssemblyAllele length
hg38191
hg19191
hg18191
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsessv8808585
SamplesNA12878
Known GenesCCS
MethodSequencing
Analysis
Platform454
Comments
Reference1000_Genomes_Consortium_Pilot_Project
Pubmed ID20981092
Accession Number(s)esv3350972
Frequency
Sample Size185
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


Hosted by The Centre for Applied Genomics
Grant support for DGV
Please read the usage disclaimer