A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv3551900



Internal ID18850181
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr16:32553179..33822829hg38UCSC Ensembl
Innerchr16:32564500..33625296hg19UCSC Ensembl
Innerchr16:32472001..33532797hg18UCSC Ensembl
Cytoband16p11.2
Allele length
AssemblyAllele length
hg381269651
hg191060797
hg181060797
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv1061140
Supporting Variants
Samples
Known GenesLOC390705, RNU6-76P, SLC6A10P, 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)nssv3551900
Frequency
Sample Size11257
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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