A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv584656



Internal ID16372065
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr2:230012405..230014629hg38UCSC Ensembl
Innerchr2:230877121..230879345hg19UCSC Ensembl
Innerchr2:230585365..230587589hg18UCSC Ensembl
Cytoband2q36.3
Allele length
AssemblyAllele length
hg382225
hg192225
hg182225
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv7331n54
Supporting Variantsnssv933581, nssv933582
Samples
Known GenesFBXO36
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nsv584656
Frequency
Sample Size17421
Observed Gain0
Observed Loss2
Observed Complex0
Frequencyn/a


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