A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1039416



Internal ID18781947
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr16:18284986..18730776hg38UCSC Ensembl
Innerchr16:18378843..18742098hg19UCSC Ensembl
Innerchr16:18286344..18649599hg18UCSC Ensembl
Cytoband16p12.3
Allele length
AssemblyAllele length
hg38445791
hg19363256
hg18363256
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv2784n100
Supporting Variantsnssv3558115, nssv3716921
Samples
Known GenesABCC6P1, LOC100288162, MIR3179-1, MIR3179-2, MIR3179-3, MIR3180-1, MIR3180-2, MIR3180-3, MIR6511A-2, MIR6770-2, NOMO2, NPIPA7, NPIPA8
MethodSNP array
AnalysisAffymetrix SNP array copy number analysis
PlatformAffymetrix SNP Array 6.0
Comments
ReferenceCoe_et_al_2014
Pubmed ID25217958
Accession Number(s)nsv1039416
Frequency
Sample Size29084
Observed Gain2
Observed Loss0
Observed Complex0
Frequencyn/a


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