A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv863121



Internal ID15810391
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 StatusS
Merged Variantsnsv573698
Supporting Variants
Samples
Known GenesCDT1
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nssv863121
Frequency
Sample Size17421
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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