A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv517801



Internal ID15445094
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr3:14220770..14240867hg38UCSC Ensembl
Innerchr3:14262270..14282367hg19UCSC Ensembl
Innerchr3:14237274..14257371hg18UCSC Ensembl
Innerchr3:14237274..14257371hg17UCSC Ensembl
Cytoband3p25.1
Allele length
AssemblyAllele length
hg3820098
hg1920098
hg1820098
hg1720098
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv695204
Samples
Known Genes
MethodSNP array
AnalysisSample-level CNVs
PlatformGPL6434
Comments
ReferenceShaikh_et_al_2009
Pubmed ID19592680
Accession Number(s)nsv517801
Frequency
Sample Size2026
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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