A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv525436



Internal ID15106043
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr3:9390066..9437458hg38UCSC Ensembl
Innerchr3:9431750..9479142hg19UCSC Ensembl
Innerchr3:9406750..9454142hg18UCSC Ensembl
Innerchr3:9406750..9454142hg17UCSC Ensembl
Cytoband3p25.3
Allele length
AssemblyAllele length
hg3847393
hg1947393
hg1847393
hg1747393
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv277n21
Supporting Variantsnssv701564
Samples
Known GenesSETD5, SETD5-AS1
MethodSNP array
AnalysisSample-level CNVs
PlatformGPL6434
Comments
ReferenceShaikh_et_al_2009
Pubmed ID19592680
Accession Number(s)nsv525436
Frequency
Sample Size2026
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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