A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv610535



Internal ID16051258
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr8:15544498..15550355hg38UCSC Ensembl
Innerchr8:15402007..15407864hg19UCSC Ensembl
Innerchr8:15446378..15452235hg18UCSC Ensembl
Cytoband8p22
Allele length
AssemblyAllele length
hg385858
hg195858
hg185858
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv12015n54
Supporting Variantsnssv1106871, nssv1106868, nssv1106869, nssv1106870, nssv1106872
Samples
Known GenesTUSC3
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nsv610535
Frequency
Sample Size17421
Observed Gain0
Observed Loss5
Observed Complex0
Frequencyn/a


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