A curated catalogue of human genomic structural variation




Variant Details

Variant: essv9746140



Internal ID18373700
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 StatusS
Merged Variantsesv3547393
Supporting Variants
Samples
Known GenesSPTY2D1, SPTY2D1-AS1
MethodSequencing
Analysis
PlatformIllumina HiSeq 2000
Comments
ReferenceBoomsma_et_al_2014
Pubmed ID23714750
Accession Number(s)essv9746140
Frequency
Sample Size767
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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