A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv522389



Internal ID15449682
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr14:76839165..76840190hg38UCSC Ensembl
Innerchr14:77305508..77306533hg19UCSC Ensembl
Innerchr14:76375261..76376286hg18UCSC Ensembl
Innerchr14:76375261..76376286hg17UCSC Ensembl
Cytoband14q24.3
Allele length
AssemblyAllele length
hg381026
hg191026
hg181026
hg171026
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv695169
Samples
Known GenesC14orf166B
MethodSNP array
AnalysisSample-level CNVs
PlatformGPL6434
Comments
ReferenceShaikh_et_al_2009
Pubmed ID19592680
Accession Number(s)nsv522389
Frequency
Sample Size2026
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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