A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv573699



Internal ID16014422
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr16:88796086..88806103hg38UCSC Ensembl
Innerchr16:88862494..88872511hg19UCSC Ensembl
Innerchr16:87389995..87400012hg18UCSC Ensembl
Cytoband16q24.3
Allele length
AssemblyAllele length
hg3810018
hg1910018
hg1810018
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv5313n54
Supporting Variantsnssv863122
Samples
Known GenesCDT1
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nsv573699
Frequency
Sample Size17421
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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