A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv518366



Internal ID15445659
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr3:172706385..172710992hg38UCSC Ensembl
Innerchr3:172424175..172428782hg19UCSC Ensembl
Innerchr3:173906869..173911476hg18UCSC Ensembl
Innerchr3:173906877..173911484hg17UCSC Ensembl
Cytoband3q26.31
Allele length
AssemblyAllele length
hg384608
hg194608
hg184608
hg174608
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv695792
Samples
Known GenesNCEH1
MethodSNP array
AnalysisSample-level CNVs
PlatformGPL6434
Comments
ReferenceShaikh_et_al_2009
Pubmed ID19592680
Accession Number(s)nsv518366
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