A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv2955061



Internal ID15440860
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 Number1
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv514477
Supporting Variants
SamplesNA21399
Known GenesTUSC3
MethodOligo aCGH
AnalysisADM2 threshold = 5
PlatformAgilent Eichler Human CNP 180K v3.0
Comments
ReferenceCampbell_et_al_2011
Pubmed ID21397061
Accession Number(s)nssv2955061
Frequency
Sample Size2366
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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