A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv520348



Internal ID15100955
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr8:18754954..18755102hg38UCSC Ensembl
Innerchr8:18612464..18612612hg19UCSC Ensembl
Innerchr8:18656744..18656892hg18UCSC Ensembl
Innerchr8:18656744..18656892hg17UCSC Ensembl
Cytoband8p22
Allele length
AssemblyAllele length
hg38149
hg19149
hg18149
hg17149
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv663098, nssv688625
Samples
Known GenesPSD3
MethodSNP array
AnalysisSample-level CNVs
PlatformGPL6434
Comments
ReferenceShaikh_et_al_2009
Pubmed ID19592680
Accession Number(s)nsv520348
Frequency
Sample Size2026
Observed Gain0
Observed Loss2
Observed Complex0
Frequencyn/a


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