A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1066169



Internal ID18808700
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr16:32081501..33535645hg38UCSC Ensembl
Innerchr16:32092822..33338112hg19UCSC Ensembl
Innerchr16:32000323..33245613hg18UCSC Ensembl
Cytoband16p11.2
Allele length
AssemblyAllele length
hg381454145
hg191245291
hg181245291
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv2839n100
Supporting Variantsnssv3549387
Samples
Known GenesHERC2P4, LOC390705, 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)nsv1066169
Frequency
Sample Size29084
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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