A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv525142



Internal ID15452435
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr5:10066978..10104856hg38UCSC Ensembl
Innerchr5:10067090..10104968hg19UCSC Ensembl
Innerchr5:10120090..10157968hg18UCSC Ensembl
Innerchr5:10120090..10157968hg17UCSC Ensembl
Cytoband5p15.2
Allele length
AssemblyAllele length
hg3837879
hg1937879
hg1837879
hg1737879
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv701212
Samples
Known Genes
MethodSNP array
AnalysisSample-level CNVs
PlatformGPL6434
Comments
ReferenceShaikh_et_al_2009
Pubmed ID19592680
Accession Number(s)nsv525142
Frequency
Sample Size2026
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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