A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv523331



Internal ID15103938
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr3:177817960..177836416hg38UCSC Ensembl
Innerchr3:177535748..177554204hg19UCSC Ensembl
Innerchr3:179018442..179036898hg18UCSC Ensembl
Innerchr3:179018450..179036906hg17UCSC Ensembl
Cytoband3q26.32
Allele length
AssemblyAllele length
hg3818457
hg1918457
hg1818457
hg1718457
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv699077
Samples
Known Genes
MethodSNP array
AnalysisSample-level CNVs
PlatformGPL6434
Comments
ReferenceShaikh_et_al_2009
Pubmed ID19592680
Accession Number(s)nsv523331
Frequency
Sample Size2026
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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