A curated catalogue of human genomic structural variation




Variant Details

Variant: esv3547393



Internal ID18401783
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr11:18608921..18608986hg38UCSC Ensembl
chr11:18630468..18630533hg19UCSC Ensembl
Cytoband11p15.1
Allele length
AssemblyAllele length
hg3866
hg1966
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsessv9746140
Samples
Known GenesSPTY2D1, SPTY2D1-AS1
MethodSequencing
Analysis
PlatformIllumina HiSeq 2000
Comments
ReferenceBoomsma_et_al_2014
Pubmed ID23714750
Accession Number(s)esv3547393
Frequency
Sample Size767
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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