A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1017621



Internal ID18760155
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr6:108524796..108569702hg38UCSC Ensembl
Innerchr6:108845999..108890905hg19UCSC Ensembl
Innerchr6:108952692..108997598hg18UCSC Ensembl
Cytoband6q21
Allele length
AssemblyAllele length
hg3844907
hg1944907
hg1844907
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv3654285
Samples
Known GenesFOXO3
MethodSNP array
AnalysisAffymetrix SNP array copy number analysis
PlatformAffymetrix SNP Array 6.0
Comments
ReferenceCoe_et_al_2014
Pubmed ID25217958
Accession Number(s)nsv1017621
Frequency
Sample Size29084
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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