A curated catalogue of human genomic structural variation




Variant Details

Variant: essv9746627



Internal ID18720873
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr11:62177360..62177610hg38UCSC Ensembl
Outerchr11:62177295..62177628hg38UCSC Ensembl
Innerchr11:61944832..61945082hg19UCSC Ensembl
Outerchr11:61944767..61945100hg19UCSC Ensembl
Cytoband11q12.3
Allele length
AssemblyAllele length
hg38334
hg19334
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsesv3547880
Supporting Variants
Samples
Known Genes
MethodSequencing
Analysis
PlatformIllumina HiSeq 2000
Comments
ReferenceBoomsma_et_al_2014
Pubmed ID23714750
Accession Number(s)essv9746627
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