A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1066580



Internal ID18809111
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr16:32047162..33822829hg38UCSC Ensembl
Innerchr16:32058483..33625296hg19UCSC Ensembl
Innerchr16:31965984..33532797hg18UCSC Ensembl
Cytoband16p11.2
Allele length
AssemblyAllele length
hg381775668
hg191566814
hg181566814
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv2839n100
Supporting Variantsnssv3716227
Samples
Known GenesHERC2P4, LOC390705, RNU6-76P, SLC6A10P, TP53TG3, TP53TG3B, TP53TG3C, TP53TG3D
MethodSNP array
AnalysisAffymetrix SNP array copy number analysis
PlatformAffymetrix SNP Array 6.0
Comments
ReferenceCoe_et_al_2014
Pubmed ID25217958
Accession Number(s)nsv1066580
Frequency
Sample Size29084
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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