A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1060660



Internal ID19149879
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr16:32447067..33813659hg38UCSC Ensembl
Innerchr16:32458388..33616126hg19UCSC Ensembl
Innerchr16:32365889..33523627hg18UCSC Ensembl
Cytoband16p11.2
Allele length
AssemblyAllele length
hg381366593
hg191157739
hg181157739
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv2871n100
Supporting Variantsnssv3551291
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)nsv1060660
Frequency
Sample Size11257
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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