A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv590711



Internal ID16378120
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr3:75519282..75869718hg38UCSC Ensembl
Innerchr3:75568433..75918869hg19UCSC Ensembl
Innerchr3:75651123..76001559hg18UCSC Ensembl
Cytoband3p12.3
Allele length
AssemblyAllele length
hg38350437
hg19350437
hg18350437
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv8385n54
Supporting Variantsnssv965798
Samples
Known GenesFLJ20518, FRG2C, LINC00960, MIR1324, MIR4273, ZNF717
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nsv590711
Frequency
Sample Size17421
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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