A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv518909



Internal ID15446202
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr14:48848846..48855744hg38UCSC Ensembl
Innerchr14:49318049..49324947hg19UCSC Ensembl
Innerchr14:48387799..48394697hg18UCSC Ensembl
Innerchr14:48387799..48394697hg17UCSC Ensembl
Cytoband14q21.3
Allele length
AssemblyAllele length
hg386899
hg196899
hg186899
hg176899
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv696369
Samples
Known Genes
MethodSNP array
AnalysisSample-level CNVs
PlatformGPL6434
Comments
ReferenceShaikh_et_al_2009
Pubmed ID19592680
Accession Number(s)nsv518909
Frequency
Sample Size2026
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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