A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv516218



Internal ID15096825
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr4:152308716..152388386hg38UCSC Ensembl
Innerchr4:153229868..153309538hg19UCSC Ensembl
Innerchr4:153449318..153528988hg18UCSC Ensembl
Innerchr4:153587473..153667143hg17UCSC Ensembl
Cytoband4q31.3
Allele length
AssemblyAllele length
hg3879671
hg1979671
hg1879671
hg1779671
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv695955, nssv660720, nssv669389, nssv663248, nssv673006, nssv652641
Samples
Known GenesDEAR, FBXW7
MethodSNP array
AnalysisSample-level CNVs
PlatformGPL6434
Comments
ReferenceShaikh_et_al_2009
Pubmed ID19592680
Accession Number(s)nsv516218
Frequency
Sample Size2026
Observed Gain0
Observed Loss6
Observed Complex0
Frequencyn/a


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