A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv520397



Internal ID15447690
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr3:173530352..173592049hg38UCSC Ensembl
Innerchr3:173248142..173309839hg19UCSC Ensembl
Innerchr3:174730836..174792533hg18UCSC Ensembl
Innerchr3:174730844..174792541hg17UCSC Ensembl
Cytoband3q26.31
Allele length
AssemblyAllele length
hg3861698
hg1961698
hg1861698
hg1761698
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv304n21
Supporting Variantsnssv697391
Samples
Known GenesNLGN1
MethodSNP array
AnalysisSample-level CNVs
PlatformGPL6434
Comments
ReferenceShaikh_et_al_2009
Pubmed ID19592680
Accession Number(s)nsv520397
Frequency
Sample Size2026
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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