A curated catalogue of human genomic structural variation




Variant Details

Variant: esv3548363



Internal ID18402753
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr11:113935098..113935459hg38UCSC Ensembl
Outerchr11:113935087..113935472hg38UCSC Ensembl
Innerchr11:113805820..113806181hg19UCSC Ensembl
Outerchr11:113805809..113806194hg19UCSC Ensembl
Cytoband11q23.2
Allele length
AssemblyAllele length
hg38386
hg19386
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsessv9747110
Samples
Known GenesHTR3B
MethodSequencing
Analysis
PlatformIllumina HiSeq 2000
Comments
ReferenceBoomsma_et_al_2014
Pubmed ID23714750
Accession Number(s)esv3548363
Frequency
Sample Size767
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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