A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv3559385



Internal ID18857666
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr16:63473412..63516342hg38UCSC Ensembl
Innerchr16:63507316..63550246hg19UCSC Ensembl
Innerchr16:62064817..62107747hg18UCSC Ensembl
Cytoband16q21
Allele length
AssemblyAllele length
hg3842931
hg1942931
hg1842931
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv1063920
Supporting Variants
Samples
Known Genes
MethodSNP array
AnalysisAffymetrix SNP array copy number analysis
PlatformAffymetrix SNP Array 6.0
Comments
ReferenceCoe_et_al_2014
Pubmed ID25217958
Accession Number(s)nssv3559385
Frequency
Sample Size11257
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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