A curated catalogue of human genomic structural variation




Variant Details

Variant: essv9752262



Internal ID18726508
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr16:59405585..59405637hg38UCSC Ensembl
chr16:59439489..59439541hg19UCSC Ensembl
Cytoband16q21
Allele length
AssemblyAllele length
hg3853
hg1953
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsesv3553515
Supporting Variants
Samples
Known Genes
MethodSequencing
Analysis
PlatformIllumina HiSeq 2000
Comments
ReferenceBoomsma_et_al_2014
Pubmed ID23714750
Accession Number(s)essv9752262
Frequency
Sample Size767
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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