A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1066889



Internal ID19156108
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr16:32217659..33970586hg38UCSC Ensembl
Innerchr16:32228980..33773053hg19UCSC Ensembl
Innerchr16:32136481..33680554hg18UCSC Ensembl
Cytoband16p11.2
Allele length
AssemblyAllele length
hg381752928
hg191544074
hg181544074
Variant TypeCNV gain+loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv2844n100
Supporting Variantsnssv3550468, nssv3716333, nssv3550461, nssv3550463, nssv3550469, nssv3550464, nssv3550462, nssv3550466, nssv3716330, nssv3716334, nssv3716331, nssv3550467, nssv3550465, nssv3550470, nssv3550473, nssv3716332, nssv3550471, nssv3550472, nssv3716329
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)nsv1066889
Frequency
Sample Size11257
Observed Gain16
Observed Loss3
Observed Complex0
Frequencyn/a


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