A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv584659



Internal ID16372068
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr2:230012456..230013964hg38UCSC Ensembl
Innerchr2:230877172..230878680hg19UCSC Ensembl
Innerchr2:230585416..230586924hg18UCSC Ensembl
Cytoband2q36.3
Allele length
AssemblyAllele length
hg381509
hg191509
hg181509
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv7333n54
Supporting Variantsnssv933588, nssv933590, nssv933585, nssv933586, nssv933589, nssv933587
Samples
Known GenesFBXO36
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nsv584659
Frequency
Sample Size17421
Observed Gain0
Observed Loss6
Observed Complex0
Frequencyn/a


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