A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv528783



Internal ID15456076
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr14:81662492..81680194hg38UCSC Ensembl
Innerchr14:82128836..82146538hg19UCSC Ensembl
Innerchr14:81198589..81216291hg18UCSC Ensembl
Innerchr14:81198589..81216291hg17UCSC Ensembl
Cytoband14q31.1
Allele length
AssemblyAllele length
hg3817703
hg1917703
hg1817703
hg1717703
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv705450
Samples
Known Genes
MethodSNP array
AnalysisSample-level CNVs
PlatformGPL6434
Comments
ReferenceShaikh_et_al_2009
Pubmed ID19592680
Accession Number(s)nsv528783
Frequency
Sample Size2026
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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