A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv3549339



Internal ID18500934
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr16:32069540..32868451hg38UCSC Ensembl
Innerchr16:32080861..32879772hg19UCSC Ensembl
Innerchr16:31988362..32787273hg18UCSC Ensembl
Cytoband16p11.2
Allele length
AssemblyAllele length
hg38798912
hg19798912
hg18798912
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv1060799
Supporting Variants
Samples
Known GenesHERC2P4, LOC390705, 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)nssv3549339
Frequency
Sample Size29084
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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