A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv573284



Internal ID16360693
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr16:79052900..79061951hg38UCSC Ensembl
Innerchr16:79086797..79095848hg19UCSC Ensembl
Innerchr16:77644298..77653349hg18UCSC Ensembl
Cytoband16q23.1
Allele length
AssemblyAllele length
hg389052
hg199052
hg189052
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv1149300
SamplesHGDP00765
Known GenesWWOX
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nsv573284
Frequency
Sample Size17421
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


Hosted by The Centre for Applied Genomics
Grant support for DGV
Please read the usage disclaimer