A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv584663



Internal ID16372072
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr2:230012561..230013964hg38UCSC Ensembl
Innerchr2:230877277..230878680hg19UCSC Ensembl
Innerchr2:230585521..230586924hg18UCSC Ensembl
Cytoband2q36.3
Allele length
AssemblyAllele length
hg381404
hg191404
hg181404
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv7333n54
Supporting Variantsnssv933603
Samples
Known GenesFBXO36
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nsv584663
Frequency
Sample Size17421
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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