A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv526099



Internal ID15453392
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr14:104276611..104325917hg38UCSC Ensembl
Innerchr14:104742948..104792254hg19UCSC Ensembl
Innerchr14:103813993..103863299hg18UCSC Ensembl
Innerchr14:103813993..103863299hg17UCSC Ensembl
Cytoband14q32.33
Allele length
AssemblyAllele length
hg3849307
hg1949307
hg1849307
hg1749307
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv702347
Samples
Known Genes
MethodSNP array
AnalysisSample-level CNVs
PlatformGPL6434
Comments
ReferenceShaikh_et_al_2009
Pubmed ID19592680
Accession Number(s)nsv526099
Frequency
Sample Size2026
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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