A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1064866



Internal ID19154085
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr16:32269023..33002529hg38UCSC Ensembl
Innerchr16:32280344..33013850hg19UCSC Ensembl
Innerchr16:32187845..32921351hg18UCSC Ensembl
Cytoband16p11.2
Allele length
AssemblyAllele length
hg38733507
hg19733507
hg18733507
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv2854n100
Supporting Variantsnssv3550551, nssv3550550
Samples
Known GenesLOC390705, 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)nsv1064866
Frequency
Sample Size11257
Observed Gain2
Observed Loss0
Observed Complex0
Frequencyn/a


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