A curated catalogue of human genomic structural variation




Variant Details

Variant: esv3553918



Internal ID18408308
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr16:89901485..89902657hg38UCSC Ensembl
Outerchr16:89901367..89902855hg38UCSC Ensembl
Innerchr16:89967893..89969065hg19UCSC Ensembl
Outerchr16:89967775..89969263hg19UCSC Ensembl
Cytoband16q24.3
Allele length
AssemblyAllele length
hg381489
hg191489
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsessv9752665
Samples
Known GenesTCF25
MethodSequencing
Analysis
PlatformIllumina HiSeq 2000
Comments
ReferenceBoomsma_et_al_2014
Pubmed ID23714750
Accession Number(s)esv3553918
Frequency
Sample Size767
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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