A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1065059



Internal ID19154278
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr16:32198766..32732148hg38UCSC Ensembl
Innerchr16:32210087..32743469hg19UCSC Ensembl
Innerchr16:32117588..32650970hg18UCSC Ensembl
Cytoband16p11.2
Allele length
AssemblyAllele length
hg38533383
hg19533383
hg18533383
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv2851n100
Supporting Variantsnssv3550418
Samples
Known GenesLOC390705, 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)nsv1065059
Frequency
Sample Size11257
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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