A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv3654285



Internal ID18605880
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 StatusS
Merged Variantsnsv1017621
Supporting Variants
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)nssv3654285
Frequency
Sample Size29084
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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