A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv526060



Internal ID15106667
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr5:31410199..31410521hg38UCSC Ensembl
Innerchr5:31410306..31410628hg19UCSC Ensembl
Innerchr5:31446063..31446385hg18UCSC Ensembl
Innerchr5:31446063..31446385hg17UCSC Ensembl
Cytoband5p13.3
Allele length
AssemblyAllele length
hg38323
hg19323
hg18323
hg17323
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv340n21
Supporting Variantsnssv702298
Samples
Known GenesDROSHA
MethodSNP array
AnalysisSample-level CNVs
PlatformGPL6434
Comments
ReferenceShaikh_et_al_2009
Pubmed ID19592680
Accession Number(s)nsv526060
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