A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1056832



Internal ID19146051
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr16:32421720..33795129hg38UCSC Ensembl
Innerchr16:32433041..33597596hg19UCSC Ensembl
Innerchr16:32340542..33505097hg18UCSC Ensembl
Cytoband16p11.2
Allele length
AssemblyAllele length
hg381373410
hg191164556
hg181164556
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv2871n100
Supporting Variantsnssv3551272
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)nsv1056832
Frequency
Sample Size11257
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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