A curated catalogue of human genomic structural variation




Variant Details

Variant: dgv5309n54



Internal ID20138733
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr16:88572446..88575640hg38UCSC Ensembl
chr16:88638854..88642048hg19UCSC Ensembl
chr16:87166355..87169549hg18UCSC Ensembl
Cytoband16q24.2
Allele length
AssemblyAllele length
hg383195
hg193195
hg183195
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnsv573667, nsv573669, nsv573670, nsv573671, nsv573664, nsv573666, nsv573665, nsv573663, nsv573662
Samples
Known GenesZC3H18
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)dgv5309n54
Frequency
Sample Size17421
Observed Gain0
Observed Loss71
Observed Complex0
Frequencyn/a


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