A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv3557059



Internal ID18508654
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr16:6814336..6878433hg38UCSC Ensembl
Innerchr16:6864337..6928434hg19UCSC Ensembl
Innerchr16:6804338..6868435hg18UCSC Ensembl
Cytoband16p13.2
Allele length
AssemblyAllele length
hg3864098
hg1964098
hg1864098
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv1039567
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)nssv3557059
Frequency
Sample Size29084
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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