A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv526039



Internal ID15106646
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr3:9390066..9453435hg38UCSC Ensembl
Innerchr3:9431750..9495119hg19UCSC Ensembl
Innerchr3:9406750..9470119hg18UCSC Ensembl
Innerchr3:9406750..9470119hg17UCSC Ensembl
Cytoband3p25.3
Allele length
AssemblyAllele length
hg3863370
hg1963370
hg1863370
hg1763370
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv277n21
Supporting Variantsnssv702272
Samples
Known GenesSETD5, SETD5-AS1
MethodSNP array
AnalysisSample-level CNVs
PlatformGPL6434
Comments
ReferenceShaikh_et_al_2009
Pubmed ID19592680
Accession Number(s)nsv526039
Frequency
Sample Size2026
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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