A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1061490



Internal ID18804021
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr16:69990674..70200621hg38UCSC Ensembl
Innerchr16:70024577..70234524hg19UCSC Ensembl
Innerchr16:68582078..68792025hg18UCSC Ensembl
Cytoband16q22.1
Allele length
AssemblyAllele length
hg38209948
hg19209948
hg18209948
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv3006n100
Supporting Variantsnssv3559482
Samples
Known GenesCLEC18C, MIR1972-1, 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)nsv1061490
Frequency
Sample Size29084
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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