A curated catalogue of human genomic structural variation




Variant Details

Variant: esv3545326



Internal ID18399716
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr9:111911905..111911962hg38UCSC Ensembl
chr9:114674185..114674242hg19UCSC Ensembl
Cytoband9q31.3
Allele length
AssemblyAllele length
hg3858
hg1958
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsessv9744073
Samples
Known GenesUGCG
MethodSequencing
Analysis
PlatformIllumina HiSeq 2000
Comments
ReferenceBoomsma_et_al_2014
Pubmed ID23714750
Accession Number(s)esv3545326
Frequency
Sample Size767
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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