A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv519028



Internal ID15099635
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr8:18847922..18866050hg38UCSC Ensembl
Innerchr8:18705432..18723560hg19UCSC Ensembl
Innerchr8:18749712..18767840hg18UCSC Ensembl
Innerchr8:18749712..18767840hg17UCSC Ensembl
Cytoband8p22
Allele length
AssemblyAllele length
hg3818129
hg1918129
hg1818129
hg1718129
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv696497
Samples
Known GenesPSD3
MethodSNP array
AnalysisSample-level CNVs
PlatformGPL6434
Comments
ReferenceShaikh_et_al_2009
Pubmed ID19592680
Accession Number(s)nsv519028
Frequency
Sample Size2026
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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