A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv520533



Internal ID15447826
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr3:142698228..142721457hg38UCSC Ensembl
Innerchr3:142417070..142440299hg19UCSC Ensembl
Innerchr3:143899760..143922989hg18UCSC Ensembl
Innerchr3:143899768..143922997hg17UCSC Ensembl
Cytoband3q23
Allele length
AssemblyAllele length
hg3823230
hg1923230
hg1823230
hg1723230
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv672770, nssv672185
Samples
Known GenesPLS1
MethodSNP array
AnalysisSample-level CNVs
PlatformGPL6434
Comments
ReferenceShaikh_et_al_2009
Pubmed ID19592680
Accession Number(s)nsv520533
Frequency
Sample Size2026
Observed Gain2
Observed Loss0
Observed Complex0
Frequencyn/a


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