A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv529013



Internal ID15456306
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr3:143158385..143169201hg38UCSC Ensembl
Innerchr3:142877227..142888043hg19UCSC Ensembl
Innerchr3:144359917..144370733hg18UCSC Ensembl
Innerchr3:144359925..144370741hg17UCSC Ensembl
Cytoband3q23
Allele length
AssemblyAllele length
hg3810817
hg1910817
hg1810817
hg1710817
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv705724
Samples
Known Genes
MethodSNP array
AnalysisSample-level CNVs
PlatformGPL6434
Comments
ReferenceShaikh_et_al_2009
Pubmed ID19592680
Accession Number(s)nsv529013
Frequency
Sample Size2026
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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