A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1058568



Internal ID18801099
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr16:32217659..34161490hg38UCSC Ensembl
Innerchr16:32228980..33963957hg19UCSC Ensembl
Innerchr16:32136481..33871458hg18UCSC Ensembl
Cytoband16p11.2
Allele length
AssemblyAllele length
hg381943832
hg191734978
hg181734978
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv2840n100
Supporting Variantsnssv3550482
Samples
Known GenesLINC00273, 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)nsv1058568
Frequency
Sample Size29084
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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