A curated catalogue of human genomic structural variation




Variant Details

Variant: esv1007865



Internal ID7072958
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 Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsessv3586691
SamplesHuRef
Known GenesZCCHC14
MethodOligo aCGH
Analysis
PlatformNot Submitted
Comments
ReferencePang_et_al_2010
Pubmed ID20482838
Accession Number(s)esv1007865
Frequency
Sample Size3
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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