A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv591829



Internal ID16032552
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr3:135388836..136050164hg38UCSC Ensembl
Innerchr3:135107678..135769006hg19UCSC Ensembl
Innerchr3:136590368..137251696hg18UCSC Ensembl
Cytoband3q22.2
Allele length
AssemblyAllele length
hg38661329
hg19661329
hg18661329
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv1152024
SamplesHGDP00761
Known GenesPPP2R3A
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nsv591829
Frequency
Sample Size17421
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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