A curated catalogue of human genomic structural variation




Variant Details

Variant: essv9752252



Internal ID18726498
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr16:58912216..58920096hg38UCSC Ensembl
Outerchr16:58911597..58920596hg38UCSC Ensembl
Innerchr16:58946120..58954000hg19UCSC Ensembl
Outerchr16:58945501..58954500hg19UCSC Ensembl
Cytoband16q21
Allele length
AssemblyAllele length
hg389000
hg199000
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsesv3553505
Supporting Variants
Samples
Known Genes
MethodSequencing
Analysis
PlatformIllumina HiSeq 2000
Comments
ReferenceBoomsma_et_al_2014
Pubmed ID23714750
Accession Number(s)essv9752252
Frequency
Sample Size767
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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