A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv933584



Internal ID16227540
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr2:230012456..230013398hg38UCSC Ensembl
Innerchr2:230877172..230878114hg19UCSC Ensembl
Innerchr2:230585416..230586358hg18UCSC Ensembl
Cytoband2q36.3
Allele length
AssemblyAllele length
hg38943
hg19943
hg18943
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv584658
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)nssv933584
Frequency
Sample Size17421
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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