A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv590809



Internal ID16378218
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr3:83120825..83256297hg38UCSC Ensembl
Innerchr3:83169976..83305448hg19UCSC Ensembl
Innerchr3:83252666..83388138hg18UCSC Ensembl
Cytoband3p12.2
Allele length
AssemblyAllele length
hg38135473
hg19135473
hg18135473
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv1152488
SamplesHGDP00947
Known Genes
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nsv590809
Frequency
Sample Size17421
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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