A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv521402



Internal ID15448695
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr4:777799..799975hg38UCSC Ensembl
Innerchr4:771587..793763hg19UCSC Ensembl
Innerchr4:761587..783763hg18UCSC Ensembl
Innerchr4:761417..783593hg17UCSC Ensembl
Cytoband4p16.3
Allele length
AssemblyAllele length
hg3822177
hg1922177
hg1822177
hg1722177
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv698012
Samples
Known GenesCPLX1, LOC100129917
MethodSNP array
AnalysisSample-level CNVs
PlatformGPL6434
Comments
ReferenceShaikh_et_al_2009
Pubmed ID19592680
Accession Number(s)nsv521402
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