A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv3550498



Internal ID18848779
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 StatusS
Merged Variantsnsv1059129
Supporting Variants
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)nssv3550498
Frequency
Sample Size11257
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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