A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv519641



Internal ID15100248
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr14:102885192..102895680hg38UCSC Ensembl
Innerchr14:103351529..103362017hg19UCSC Ensembl
Innerchr14:102421282..102431770hg18UCSC Ensembl
Innerchr14:102421282..102431770hg17UCSC Ensembl
Cytoband14q32.32
Allele length
AssemblyAllele length
hg3810489
hg1910489
hg1810489
hg1710489
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv657314, nssv687721
Samples
Known GenesTRAF3
MethodSNP array
AnalysisSample-level CNVs
PlatformGPL6434
Comments
ReferenceShaikh_et_al_2009
Pubmed ID19592680
Accession Number(s)nsv519641
Frequency
Sample Size2026
Observed Gain0
Observed Loss2
Observed Complex0
Frequencyn/a


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