A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv3557014



Internal ID18508609
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr16:6031911..6059326hg38UCSC Ensembl
Innerchr16:6081912..6109327hg19UCSC Ensembl
Innerchr16:6021913..6049328hg18UCSC Ensembl
Cytoband16p13.3
Allele length
AssemblyAllele length
hg3827416
hg1927416
hg1827416
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv1036797
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)nssv3557014
Frequency
Sample Size29084
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


Hosted by The Centre for Applied Genomics
Grant support for DGV
Please read the usage disclaimer