A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv573698



Internal ID16014421
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr16:88796086..88804814hg38UCSC Ensembl
Innerchr16:88862494..88871222hg19UCSC Ensembl
Innerchr16:87389995..87398723hg18UCSC Ensembl
Cytoband16q24.3
Allele length
AssemblyAllele length
hg388729
hg198729
hg188729
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv5313n54
Supporting Variantsnssv863121
Samples
Known GenesCDT1
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nsv573698
Frequency
Sample Size17421
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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