A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv519225



Internal ID15446518
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr17:12156934..12177087hg38UCSC Ensembl
Innerchr17:12060251..12080404hg19UCSC Ensembl
Innerchr17:12000976..12021129hg18UCSC Ensembl
Innerchr17:12000976..12021129hg17UCSC Ensembl
Cytoband17p12
Allele length
AssemblyAllele length
hg3820154
hg1920154
hg1820154
hg1720154
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv177n21
Supporting Variantsnssv696715
Samples
Known Genes
MethodSNP array
AnalysisSample-level CNVs
PlatformGPL6434
Comments
ReferenceShaikh_et_al_2009
Pubmed ID19592680
Accession Number(s)nsv519225
Frequency
Sample Size2026
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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