A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv610545



Internal ID16051268
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr8:15545427..15554587hg38UCSC Ensembl
Innerchr8:15402936..15412096hg19UCSC Ensembl
Innerchr8:15447307..15456467hg18UCSC Ensembl
Cytoband8p22
Allele length
AssemblyAllele length
hg389161
hg199161
hg189161
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv12014n54
Supporting Variantsnssv1106914, nssv1106913, nssv1106917, nssv1106916, nssv1106915, nssv1106912, nssv1106918
Samples
Known GenesTUSC3
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nsv610545
Frequency
Sample Size17421
Observed Gain0
Observed Loss7
Observed Complex0
Frequencyn/a


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