A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv1106902



Internal ID15613402
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr8:15545427..15550355hg38UCSC Ensembl
Innerchr8:15402936..15407864hg19UCSC Ensembl
Innerchr8:15447307..15452235hg18UCSC Ensembl
Cytoband8p22
Allele length
AssemblyAllele length
hg384929
hg194929
hg184929
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv610540
Supporting Variants
Samples
Known GenesTUSC3
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nssv1106902
Frequency
Sample Size17421
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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