A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv525460



Internal ID15106067
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr14:66384467..67159877hg38UCSC Ensembl
Innerchr14:66851185..67626594hg19UCSC Ensembl
Innerchr14:65920938..66696347hg18UCSC Ensembl
Innerchr14:65920938..66696347hg17UCSC Ensembl
Cytoband14q23.3
Allele length
AssemblyAllele length
hg38775411
hg19775410
hg18775410
hg17775410
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv701588
Samples
Known GenesGPHN, LINC00238
MethodSNP array
AnalysisSample-level CNVs
PlatformGPL6434
Comments
ReferenceShaikh_et_al_2009
Pubmed ID19592680
Accession Number(s)nsv525460
Frequency
Sample Size2026
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


Hosted by The Centre for Applied Genomics
Grant support for DGV
Please read the usage disclaimer