A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv525698



Internal ID15452991
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr12:90244862..90261073hg38UCSC Ensembl
Innerchr12:90638639..90654850hg19UCSC Ensembl
Innerchr12:89162770..89178981hg18UCSC Ensembl
Innerchr12:89141107..89157318hg17UCSC Ensembl
Cytoband12q21.33
Allele length
AssemblyAllele length
hg3816212
hg1916212
hg1816212
hg1716212
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv701858
Samples
Known Genes
MethodSNP array
AnalysisSample-level CNVs
PlatformGPL6434
Comments
ReferenceShaikh_et_al_2009
Pubmed ID19592680
Accession Number(s)nsv525698
Frequency
Sample Size2026
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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