A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv3549281



Internal ID18500876
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr16:32047162..33908301hg38UCSC Ensembl
Innerchr16:32058483..33710768hg19UCSC Ensembl
Innerchr16:31965984..33618269hg18UCSC Ensembl
Cytoband16p11.2
Allele length
AssemblyAllele length
hg381861140
hg191652286
hg181652286
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv1059124
Supporting Variants
Samples
Known GenesHERC2P4, LOC390705, RNU6-76P, 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)nssv3549281
Frequency
Sample Size29084
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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