A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv3550454



Internal ID18848735
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr16:32217659..33829351hg38UCSC Ensembl
Innerchr16:32228980..33631818hg19UCSC Ensembl
Innerchr16:32136481..33539319hg18UCSC Ensembl
Cytoband16p11.2
Allele length
AssemblyAllele length
hg381611693
hg191402839
hg181402839
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv1063163
Supporting Variants
Samples
Known GenesLOC390705, 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)nssv3550454
Frequency
Sample Size11257
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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