A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv933583



Internal ID16227539
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr2:230012456..230013303hg38UCSC Ensembl
Innerchr2:230877172..230878019hg19UCSC Ensembl
Innerchr2:230585416..230586263hg18UCSC Ensembl
Cytoband2q36.3
Allele length
AssemblyAllele length
hg38848
hg19848
hg18848
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv584657
Supporting Variants
Samples
Known GenesFBXO36
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nssv933583
Frequency
Sample Size17421
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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