A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv3718898



Internal ID18670493
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr16:14741198..14965879hg38UCSC Ensembl
Innerchr16:14835055..15059736hg19UCSC Ensembl
Innerchr16:14742556..14967237hg18UCSC Ensembl
Cytoband16p13.11
Allele length
AssemblyAllele length
hg38224682
hg19224682
hg18224682
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv1050293
Supporting Variants
Samples
Known GenesABCC6P2, LOC100288162, MIR3179-1, MIR3179-2, MIR3179-3, MIR3180-1, MIR3180-2, MIR3180-3, MIR6511A-2, MIR6770-2, NOMO1, NPIPA1, NPIPA2, NPIPA3
MethodSNP array
AnalysisAffymetrix SNP array copy number analysis
PlatformAffymetrix SNP Array 6.0
Comments
ReferenceCoe_et_al_2014
Pubmed ID25217958
Accession Number(s)nssv3718898
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