A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv519605



Internal ID15100212
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr14:104080556..104191423hg38UCSC Ensembl
Innerchr14:104546893..104657760hg19UCSC Ensembl
Innerchr14:103616646..103727513hg18UCSC Ensembl
Innerchr14:103616646..103727513hg17UCSC Ensembl
Cytoband14q32.33
Allele length
AssemblyAllele length
hg38110868
hg19110868
hg18110868
hg17110868
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv685199, nssv657042
Samples
Known GenesASPG, KIF26A, MIR203, MIR3545
MethodSNP array
AnalysisSample-level CNVs
PlatformGPL6434
Comments
ReferenceShaikh_et_al_2009
Pubmed ID19592680
Accession Number(s)nsv519605
Frequency
Sample Size2026
Observed Gain0
Observed Loss2
Observed Complex0
Frequencyn/a


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