A curated catalogue of human genomic structural variation




Variant Details

Variant: essv9746720



Internal ID18720966
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr11:70229102..70237078hg38UCSC Ensembl
Outerchr11:70228373..70238894hg38UCSC Ensembl
Innerchr11:70075208..70083184hg19UCSC Ensembl
Outerchr11:70074479..70085000hg19UCSC Ensembl
Cytoband11q13.3
Allele length
AssemblyAllele length
hg3810522
hg1910522
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsesv3547973
Supporting Variants
Samples
Known Genes
MethodSequencing
Analysis
PlatformIllumina HiSeq 2000
Comments
ReferenceBoomsma_et_al_2014
Pubmed ID23714750
Accession Number(s)essv9746720
Frequency
Sample Size767
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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