A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv527401



Internal ID15454694
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr3:193420916..193434619hg38UCSC Ensembl
Innerchr3:193138705..193152408hg19UCSC Ensembl
Innerchr3:194621399..194635102hg18UCSC Ensembl
Innerchr3:194621407..194635110hg17UCSC Ensembl
Cytoband3q29
Allele length
AssemblyAllele length
hg3813704
hg1913704
hg1813704
hg1713704
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv309n21
Supporting Variantsnssv703837
Samples
Known GenesATP13A4
MethodSNP array
AnalysisSample-level CNVs
PlatformGPL6434
Comments
ReferenceShaikh_et_al_2009
Pubmed ID19592680
Accession Number(s)nsv527401
Frequency
Sample Size2026
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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