A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv584665



Internal ID16372074
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr2:230012668..230014629hg38UCSC Ensembl
Innerchr2:230877384..230879345hg19UCSC Ensembl
Innerchr2:230585628..230587589hg18UCSC Ensembl
Cytoband2q36.3
Allele length
AssemblyAllele length
hg381962
hg191962
hg181962
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv7331n54
Supporting Variantsnssv933605
Samples
Known GenesFBXO36
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nsv584665
Frequency
Sample Size17421
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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