A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv525569



Internal ID15452862
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr4:24645149..24694860hg38UCSC Ensembl
Innerchr4:24646772..24696483hg19UCSC Ensembl
Innerchr4:24255870..24305581hg18UCSC Ensembl
Innerchr4:24323041..24372752hg17UCSC Ensembl
Cytoband4p15.2
Allele length
AssemblyAllele length
hg3849712
hg1949712
hg1849712
hg1749712
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv701708
Samples
Known Genes
MethodSNP array
AnalysisSample-level CNVs
PlatformGPL6434
Comments
ReferenceShaikh_et_al_2009
Pubmed ID19592680
Accession Number(s)nsv525569
Frequency
Sample Size2026
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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