A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv526405



Internal ID15453698
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr3:193412018..193420916hg38UCSC Ensembl
Innerchr3:193129807..193138705hg19UCSC Ensembl
Innerchr3:194612501..194621399hg18UCSC Ensembl
Innerchr3:194612509..194621407hg17UCSC Ensembl
Cytoband3q29
Allele length
AssemblyAllele length
hg388899
hg198899
hg188899
hg178899
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv702705
Samples
Known GenesATP13A4
MethodSNP array
AnalysisSample-level CNVs
PlatformGPL6434
Comments
ReferenceShaikh_et_al_2009
Pubmed ID19592680
Accession Number(s)nsv526405
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