A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv3717247



Internal ID19015528
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr16:33043325..34035419hg38UCSC Ensembl
Innerchr16:33054646..33837886hg19UCSC Ensembl
Innerchr16:32962147..33745387hg18UCSC Ensembl
Cytoband16p11.2
Allele length
AssemblyAllele length
hg38992095
hg19783241
hg18783241
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv1055989
Supporting Variants
Samples
Known GenesLOC390705, RNU6-76P, TP53TG3, TP53TG3B, TP53TG3C
MethodSNP array
AnalysisAffymetrix SNP array copy number analysis
PlatformAffymetrix SNP Array 6.0
Comments
ReferenceCoe_et_al_2014
Pubmed ID25217958
Accession Number(s)nssv3717247
Frequency
Sample Size11257
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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