A curated catalogue of human genomic structural variation




Variant Details

Variant: essv3586691



Internal ID7058073
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr16:87476501..87525887hg38UCSC Ensembl
Innerchr16:87510107..87559493hg19UCSC Ensembl
Innerchr16:86067608..86116994hg18UCSC Ensembl
Cytoband16q24.2
Allele length
AssemblyAllele length
hg3849387
hg1949387
hg1849387
Variant TypeCNV loss
Copy Number
Allele State
Allele OriginNot tested
Probe Count
Validation Flag
Merged StatusS
Merged Variantsesv1007865
Supporting Variants
SamplesHuRef
Known GenesZCCHC14
MethodOligo aCGH
Analysis
PlatformNot Submitted
Comments
ReferencePang_et_al_2010
Pubmed ID20482838
Accession Number(s)essv3586691
Frequency
Sample Size3
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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