A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv610553



Internal ID16051276
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr8:15548450..15554587hg38UCSC Ensembl
Innerchr8:15405959..15412096hg19UCSC Ensembl
Innerchr8:15450330..15456467hg18UCSC Ensembl
Cytoband8p22
Allele length
AssemblyAllele length
hg386138
hg196138
hg186138
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv12018n54
Supporting Variantsnssv1106928, nssv1106929, nssv1106927
Samples
Known GenesTUSC3
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nsv610553
Frequency
Sample Size17421
Observed Gain0
Observed Loss3
Observed Complex0
Frequencyn/a


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