A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv1106940



Internal ID15960126
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr8:15562268..15585104hg38UCSC Ensembl
Innerchr8:15419777..15442613hg19UCSC Ensembl
Innerchr8:15464148..15486984hg18UCSC Ensembl
Cytoband8p22
Allele length
AssemblyAllele length
hg3822837
hg1922837
hg1822837
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv610556
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)nssv1106940
Frequency
Sample Size17421
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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