A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv518066



Internal ID15445359
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr14:100746371..100751904hg38UCSC Ensembl
Innerchr14:101212708..101218241hg19UCSC Ensembl
Innerchr14:100282461..100287994hg18UCSC Ensembl
Innerchr14:100282461..100287994hg17UCSC Ensembl
Cytoband14q32.2
Allele length
AssemblyAllele length
hg385534
hg195534
hg185534
hg175534
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv695477
Samples
Known Genes
MethodSNP array
AnalysisSample-level CNVs
PlatformGPL6434
Comments
ReferenceShaikh_et_al_2009
Pubmed ID19592680
Accession Number(s)nsv518066
Frequency
Sample Size2026
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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