A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv3550499



Internal ID18848780
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr16:32233140..33043325hg38UCSC Ensembl
Innerchr16:32244461..33054646hg19UCSC Ensembl
Innerchr16:32151962..32962147hg18UCSC Ensembl
Cytoband16p11.2
Allele length
AssemblyAllele length
hg38810186
hg19810186
hg18810186
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv1064815
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)nssv3550499
Frequency
Sample Size11257
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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