A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv3549171



Internal ID18500766
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr16:31960187..33002529hg38UCSC Ensembl
Innerchr16:31971508..33013850hg19UCSC Ensembl
Innerchr16:31879009..32921351hg18UCSC Ensembl
Cytoband16p11.2
Allele length
AssemblyAllele length
hg381042343
hg191042343
hg181042343
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv1066252
Supporting Variants
Samples
Known GenesHERC2P4, LOC390705, 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)nssv3549171
Frequency
Sample Size29084
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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