A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv518830



Internal ID15099437
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr4:15609148..15670577hg38UCSC Ensembl
Innerchr4:15610771..15672200hg19UCSC Ensembl
Innerchr4:15219869..15281298hg18UCSC Ensembl
Innerchr4:15287040..15348469hg17UCSC Ensembl
Cytoband4p15.32
Allele length
AssemblyAllele length
hg3861430
hg1961430
hg1861430
hg1761430
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv315n21
Supporting Variantsnssv696284
Samples
Known GenesFBXL5
MethodSNP array
AnalysisSample-level CNVs
PlatformGPL6434
Comments
ReferenceShaikh_et_al_2009
Pubmed ID19592680
Accession Number(s)nsv518830
Frequency
Sample Size2026
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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