A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv604476



Internal ID16391885
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr6:108556849..108561930hg38UCSC Ensembl
Innerchr6:108878052..108883133hg19UCSC Ensembl
Innerchr6:108984745..108989826hg18UCSC Ensembl
Cytoband6q21
Allele length
AssemblyAllele length
hg385082
hg195082
hg185082
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv1071952
Samples
Known GenesFOXO3
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nsv604476
Frequency
Sample Size17421
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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