A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1062921



Internal ID18805452
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr16:32289569..33908301hg38UCSC Ensembl
Innerchr16:32300890..33710768hg19UCSC Ensembl
Innerchr16:32208391..33618269hg18UCSC Ensembl
Cytoband16p11.2
Allele length
AssemblyAllele length
hg381618733
hg191409879
hg181409879
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv2840n100
Supporting Variantsnssv3550604
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)nsv1062921
Frequency
Sample Size29084
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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