A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv590055



Internal ID16377464
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr3:35739895..35897303hg38UCSC Ensembl
Innerchr3:35781387..35938795hg19UCSC Ensembl
Innerchr3:35756391..35913799hg18UCSC Ensembl
Cytoband3p22.3
Allele length
AssemblyAllele length
hg38157409
hg19157409
hg18157409
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv962132
Samples
Known GenesARPP21, MIR128-2
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nsv590055
Frequency
Sample Size17421
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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