A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1058574



Internal ID18801105
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr16:69990674..70153279hg38UCSC Ensembl
Innerchr16:70024577..70187182hg19UCSC Ensembl
Innerchr16:68582078..68744683hg18UCSC Ensembl
Cytoband16q22.1
Allele length
AssemblyAllele length
hg38162606
hg19162606
hg18162606
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv3004n100
Supporting Variantsnssv3559475, nssv3559476, nssv3559472, nssv3559473, nssv3559474, nssv3722734
Samples
Known GenesMIR1972-1, MIR1972-2, PDPR, PDXDC2P
MethodSNP array
AnalysisAffymetrix SNP array copy number analysis
PlatformAffymetrix SNP Array 6.0
Comments
ReferenceCoe_et_al_2014
Pubmed ID25217958
Accession Number(s)nsv1058574
Frequency
Sample Size29084
Observed Gain6
Observed Loss0
Observed Complex0
Frequencyn/a


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