A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv521779



Internal ID15449072
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr14:89972636..89989844hg38UCSC Ensembl
Innerchr14:90438980..90456188hg19UCSC Ensembl
Innerchr14:89508733..89525941hg18UCSC Ensembl
Innerchr14:89508733..89525941hg17UCSC Ensembl
Cytoband14q32.11
Allele length
AssemblyAllele length
hg3817209
hg1917209
hg1817209
hg1717209
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv694546
Samples
Known GenesTDP1
MethodSNP array
AnalysisSample-level CNVs
PlatformGPL6434
Comments
ReferenceShaikh_et_al_2009
Pubmed ID19592680
Accession Number(s)nsv521779
Frequency
Sample Size2026
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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