A curated catalogue of human genomic structural variation




Variant Details

Variant: essv9752364



Internal ID18726610
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr16:69820582..69824628hg38UCSC Ensembl
Outerchr16:69820180..69824922hg38UCSC Ensembl
Innerchr16:69854485..69858531hg19UCSC Ensembl
Outerchr16:69854083..69858825hg19UCSC Ensembl
Cytoband16q22.1
Allele length
AssemblyAllele length
hg384743
hg194743
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsesv3553617
Supporting Variants
Samples
Known GenesWWP2
MethodSequencing
Analysis
PlatformIllumina HiSeq 2000
Comments
ReferenceBoomsma_et_al_2014
Pubmed ID23714750
Accession Number(s)essv9752364
Frequency
Sample Size767
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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