A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv604480



Internal ID16391889
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr6:108559544..108561883hg38UCSC Ensembl
Innerchr6:108880747..108883086hg19UCSC Ensembl
Innerchr6:108987440..108989779hg18UCSC Ensembl
Cytoband6q21
Allele length
AssemblyAllele length
hg382340
hg192340
hg182340
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv10904n54
Supporting Variantsnssv1071957
Samples
Known GenesFOXO3
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nsv604480
Frequency
Sample Size17421
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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