A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1060871



Internal ID19150090
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr16:32169453..32804488hg38UCSC Ensembl
Innerchr16:32180774..32815809hg19UCSC Ensembl
Innerchr16:32088275..32723310hg18UCSC Ensembl
Cytoband16p11.2
Allele length
AssemblyAllele length
hg38635036
hg19635036
hg18635036
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv2854n100
Supporting Variantsnssv3550375, nssv3716300
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)nsv1060871
Frequency
Sample Size11257
Observed Gain2
Observed Loss0
Observed Complex0
Frequencyn/a


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