A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv521615



Internal ID15448908
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr1:49827749..49991165hg38UCSC Ensembl
Innerchr1:50293421..50456837hg19UCSC Ensembl
Innerchr1:50066008..50229424hg18UCSC Ensembl
Innerchr1:50005441..50168857hg17UCSC Ensembl
Cytoband1p33
Allele length
AssemblyAllele length
hg38163417
hg19163417
hg18163417
hg17163417
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv698233
Samples
Known GenesAGBL4
MethodSNP array
AnalysisSample-level CNVs
PlatformGPL6434
Comments
ReferenceShaikh_et_al_2009
Pubmed ID19592680
Accession Number(s)nsv521615
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