A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv519148



Internal ID15099755
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr3:86781927..86945974hg38UCSC Ensembl
Innerchr3:86831077..86995124hg19UCSC Ensembl
Innerchr3:86913767..87077814hg18UCSC Ensembl
Innerchr3:86913767..87077814hg17UCSC Ensembl
Cytoband3p12.1
Allele length
AssemblyAllele length
hg38164048
hg19164048
hg18164048
hg17164048
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv696625
Samples
Known GenesVGLL3
MethodSNP array
AnalysisSample-level CNVs
PlatformGPL6434
Comments
ReferenceShaikh_et_al_2009
Pubmed ID19592680
Accession Number(s)nsv519148
Frequency
Sample Size2026
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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