A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv573664



Internal ID16014387
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr16:88572446..88575477hg38UCSC Ensembl
Innerchr16:88638854..88641885hg19UCSC Ensembl
Innerchr16:87166355..87169386hg18UCSC Ensembl
Cytoband16q24.2
Allele length
AssemblyAllele length
hg383032
hg193032
hg183032
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv5309n54
Supporting Variantsnssv863016
Samples
Known GenesZC3H18
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nsv573664
Frequency
Sample Size17421
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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