A curated catalogue of human genomic structural variation




Variant Details

Variant: essv9752473



Internal ID18726719
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 StatusS
Merged Variantsesv3553726
Supporting Variants
Samples
Known Genes
MethodSequencing
Analysis
PlatformIllumina HiSeq 2000
Comments
ReferenceBoomsma_et_al_2014
Pubmed ID23714750
Accession Number(s)essv9752473
Frequency
Sample Size767
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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