A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv573689



Internal ID16014412
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr16:88795879..88804559hg38UCSC Ensembl
Innerchr16:88862287..88870967hg19UCSC Ensembl
Innerchr16:87389788..87398468hg18UCSC Ensembl
Cytoband16q24.3
Allele length
AssemblyAllele length
hg388681
hg198681
hg188681
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv5313n54
Supporting Variantsnssv863102
Samples
Known GenesCDT1
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nsv573689
Frequency
Sample Size17421
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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