A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv3557016



Internal ID18508611
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr16:6123185..6138570hg38UCSC Ensembl
Innerchr16:6173186..6188571hg19UCSC Ensembl
Innerchr16:6113187..6128572hg18UCSC Ensembl
Cytoband16p13.3
Allele length
AssemblyAllele length
hg3815386
hg1915386
hg1815386
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv1038096
Supporting Variants
Samples
Known GenesRBFOX1
MethodSNP array
AnalysisAffymetrix SNP array copy number analysis
PlatformAffymetrix SNP Array 6.0
Comments
ReferenceCoe_et_al_2014
Pubmed ID25217958
Accession Number(s)nssv3557016
Frequency
Sample Size29084
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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