A curated catalogue of human genomic structural variation




Variant Details

Variant: esv3553726



Internal ID18754802
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr16:79226759..79245603hg38UCSC Ensembl
Outerchr16:79226104..79248315hg38UCSC Ensembl
Innerchr16:79260656..79279500hg19UCSC Ensembl
Outerchr16:79260001..79282212hg19UCSC Ensembl
Cytoband16q23.2
Allele length
AssemblyAllele length
hg3822212
hg1922212
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsessv9752473
Samples
Known Genes
MethodSequencing
Analysis
PlatformIllumina HiSeq 2000
Comments
ReferenceBoomsma_et_al_2014
Pubmed ID23714750
Accession Number(s)esv3553726
Frequency
Sample Size767
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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