A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1059129



Internal ID19148348
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr16:32233140..32904180hg38UCSC Ensembl
Innerchr16:32244461..32915501hg19UCSC Ensembl
Innerchr16:32151962..32823002hg18UCSC Ensembl
Cytoband16p11.2
Allele length
AssemblyAllele length
hg38671041
hg19671041
hg18671041
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv2854n100
Supporting Variantsnssv3550498
Samples
Known GenesLOC390705, 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)nsv1059129
Frequency
Sample Size11257
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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