A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv518793



Internal ID15446086
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr14:68862432..68864936hg38UCSC Ensembl
Innerchr14:69329149..69331653hg19UCSC Ensembl
Innerchr14:68398902..68401406hg18UCSC Ensembl
Innerchr14:68398902..68401406hg17UCSC Ensembl
Cytoband14q24.1
Allele length
AssemblyAllele length
hg382505
hg192505
hg182505
hg172505
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv696246
Samples
Known Genes
MethodSNP array
AnalysisSample-level CNVs
PlatformGPL6434
Comments
ReferenceShaikh_et_al_2009
Pubmed ID19592680
Accession Number(s)nsv518793
Frequency
Sample Size2026
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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