A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv526733



Internal ID15454026
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr3:86435748..86451394hg38UCSC Ensembl
Innerchr3:86484898..86500544hg19UCSC Ensembl
Innerchr3:86567588..86583234hg18UCSC Ensembl
Innerchr3:86567588..86583234hg17UCSC Ensembl
Cytoband3p12.1
Allele length
AssemblyAllele length
hg3815647
hg1915647
hg1815647
hg1715647
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv703075
Samples
Known GenesRNU6-69P
MethodSNP array
AnalysisSample-level CNVs
PlatformGPL6434
Comments
ReferenceShaikh_et_al_2009
Pubmed ID19592680
Accession Number(s)nsv526733
Frequency
Sample Size2026
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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