A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv518260



Internal ID15445553
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr14:27931350..27951885hg38UCSC Ensembl
Innerchr14:28400556..28421091hg19UCSC Ensembl
Innerchr14:27470396..27490931hg18UCSC Ensembl
Innerchr14:27470396..27490931hg17UCSC Ensembl
Cytoband14q12
Allele length
AssemblyAllele length
hg3820536
hg1920536
hg1820536
hg1720536
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv695691
Samples
Known Genes
MethodSNP array
AnalysisSample-level CNVs
PlatformGPL6434
Comments
ReferenceShaikh_et_al_2009
Pubmed ID19592680
Accession Number(s)nsv518260
Frequency
Sample Size2026
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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