A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv514477



Internal ID15466163
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr8:15545759..15569957hg38UCSC Ensembl
Innerchr8:15403268..15427466hg19UCSC Ensembl
Innerchr8:15447639..15471837hg18UCSC Ensembl
Cytoband8p22
Allele length
AssemblyAllele length
hg3824199
hg1924199
hg1824199
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv2955059, nssv2955058, nssv2955061, nssv2955060
SamplesNA21399, NA10863, NA12234, NA12766
Known GenesTUSC3
MethodOligo aCGH
AnalysisADM2 threshold = 5
PlatformAgilent Eichler Human CNP 180K v3.0
Comments
ReferenceCampbell_et_al_2011
Pubmed ID21397061
Accession Number(s)nsv514477
Frequency
Sample Size2366
Observed Gain0
Observed Loss4
Observed Complex0
Frequencyn/a


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