A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv604478



Internal ID16391887
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr6:108559308..108561883hg38UCSC Ensembl
Innerchr6:108880511..108883086hg19UCSC Ensembl
Innerchr6:108987204..108989779hg18UCSC Ensembl
Cytoband6q21
Allele length
AssemblyAllele length
hg382576
hg192576
hg182576
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv10904n54
Supporting Variantsnssv1071955, nssv1071954
Samples
Known GenesFOXO3
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nsv604478
Frequency
Sample Size17421
Observed Gain0
Observed Loss2
Observed Complex0
Frequencyn/a


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