A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1043497



Internal ID18786028
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr16:14686785..15014718hg38UCSC Ensembl
Innerchr16:14780642..15108575hg19UCSC Ensembl
Innerchr16:14688143..15016076hg18UCSC Ensembl
Cytoband16p13.11
Allele length
AssemblyAllele length
hg38327934
hg19327934
hg18327934
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv2738n100
Supporting Variantsnssv3557246
Samples
Known GenesABCC6P2, LOC100288162, MIR1972-1, MIR1972-2, MIR3179-1, MIR3179-2, MIR3179-3, MIR3180-1, MIR3180-2, MIR3180-3, MIR6511A-2, MIR6770-2, NOMO1, NPIPA1, NPIPA2, NPIPA3, PDXDC1, PLA2G10
MethodSNP array
AnalysisAffymetrix SNP array copy number analysis
PlatformAffymetrix SNP Array 6.0
Comments
ReferenceCoe_et_al_2014
Pubmed ID25217958
Accession Number(s)nsv1043497
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