A curated catalogue of human genomic structural variation




Variant Details

Variant: essv9746368



Internal ID18720614
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr11:39093953..39094243hg38UCSC Ensembl
Outerchr11:39093878..39094299hg38UCSC Ensembl
Innerchr11:39115503..39115793hg19UCSC Ensembl
Outerchr11:39115428..39115849hg19UCSC Ensembl
Cytoband11p12
Allele length
AssemblyAllele length
hg38422
hg19422
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsesv3547621
Supporting Variants
Samples
Known Genes
MethodSequencing
Analysis
PlatformIllumina HiSeq 2000
Comments
ReferenceBoomsma_et_al_2014
Pubmed ID23714750
Accession Number(s)essv9746368
Frequency
Sample Size767
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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