A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv3718986



Internal ID18670581
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr16:16149597..16170241hg38UCSC Ensembl
Innerchr16:16243454..16264098hg19UCSC Ensembl
Innerchr16:16150955..16171599hg18UCSC Ensembl
Cytoband16p13.11
Allele length
AssemblyAllele length
hg3820645
hg1920645
hg1820645
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv1045013
Supporting Variants
Samples
Known GenesABCC6
MethodSNP array
AnalysisAffymetrix SNP array copy number analysis
PlatformAffymetrix SNP Array 6.0
Comments
ReferenceCoe_et_al_2014
Pubmed ID25217958
Accession Number(s)nssv3718986
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