A curated catalogue of human genomic structural variation




Variant Details

Variant: esv3547338



Internal ID18401728
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr11:12906105..12907206hg38UCSC Ensembl
Outerchr11:12906099..12907222hg38UCSC Ensembl
Innerchr11:12927652..12928753hg19UCSC Ensembl
Outerchr11:12927646..12928769hg19UCSC Ensembl
Cytoband11p15.2
Allele length
AssemblyAllele length
hg381124
hg191124
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsessv9746085
Samples
Known GenesTEAD1
MethodSequencing
Analysis
PlatformIllumina HiSeq 2000
Comments
ReferenceBoomsma_et_al_2014
Pubmed ID23714750
Accession Number(s)esv3547338
Frequency
Sample Size767
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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