A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv518295



Internal ID15098902
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr20:1312402..1312603hg38UCSC Ensembl
Innerchr20:1293046..1293247hg19UCSC Ensembl
Innerchr20:1241046..1241247hg18UCSC Ensembl
Innerchr20:1241046..1241247hg17UCSC Ensembl
Cytoband20p13
Allele length
AssemblyAllele length
hg38202
hg19202
hg18202
hg17202
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv695726
Samples
Known GenesFKBP1A-SDCBP2, SDCBP2
MethodSNP array
AnalysisSample-level CNVs
PlatformGPL6434
Comments
ReferenceShaikh_et_al_2009
Pubmed ID19592680
Accession Number(s)nsv518295
Frequency
Sample Size2026
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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