A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv521053



Internal ID15101660
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr8:18592131..18611841hg38UCSC Ensembl
Innerchr8:18449641..18469351hg19UCSC Ensembl
Innerchr8:18493921..18513631hg18UCSC Ensembl
Innerchr8:18493921..18513631hg17UCSC Ensembl
Cytoband8p22
Allele length
AssemblyAllele length
hg3819711
hg1919711
hg1819711
hg1719711
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv680847, nssv696164, nssv697363, nssv683732
Samples
Known GenesPSD3
MethodSNP array
AnalysisSample-level CNVs
PlatformGPL6434
Comments
ReferenceShaikh_et_al_2009
Pubmed ID19592680
Accession Number(s)nsv521053
Frequency
Sample Size2026
Observed Gain4
Observed Loss0
Observed Complex0
Frequencyn/a


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