A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1067011



Internal ID19156230
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr16:32369618..33818870hg38UCSC Ensembl
Innerchr16:32380939..33621337hg19UCSC Ensembl
Innerchr16:32288440..33528838hg18UCSC Ensembl
Cytoband16p11.2
Allele length
AssemblyAllele length
hg381449253
hg191240399
hg181240399
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv2871n100
Supporting Variantsnssv3551099, nssv3551098
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)nsv1067011
Frequency
Sample Size11257
Observed Gain2
Observed Loss0
Observed Complex0
Frequencyn/a


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