A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv527954



Internal ID15108561
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr3:9407371..9437458hg38UCSC Ensembl
Innerchr3:9449055..9479142hg19UCSC Ensembl
Innerchr3:9424055..9454142hg18UCSC Ensembl
Innerchr3:9424055..9454142hg17UCSC Ensembl
Cytoband3p25.3
Allele length
AssemblyAllele length
hg3830088
hg1930088
hg1830088
hg1730088
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv704464
Samples
Known GenesSETD5
MethodSNP array
AnalysisSample-level CNVs
PlatformGPL6434
Comments
ReferenceShaikh_et_al_2009
Pubmed ID19592680
Accession Number(s)nsv527954
Frequency
Sample Size2026
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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