A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv2070111



Internal ID17518874
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr16:88165314..88194603hg38UCSC Ensembl
Innerchr16:88198920..88228209hg19UCSC Ensembl
Innerchr16:86756421..86785710hg18UCSC Ensembl
Cytoband16q24.2
Allele length
AssemblyAllele length
hg3829290
hg1929290
hg1829290
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag1
Merged StatusS
Merged Variantsnsv978177
Supporting Variants
SamplesHGDP01284
Known Genes
MethodSequencing
Analysislineage specific fixed duplications
PlatformNot reported
Commentslineage specific duplication - fixed_Ptrs-Ptrt-Ptre-Ptrv-Ppa-Hsa-Hde
ReferenceSudmant_et_al_2013
Pubmed ID23825009
Accession Number(s)nssv2070111
Frequency
Sample Size10
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


Hosted by The Centre for Applied Genomics
Grant support for DGV
Please read the usage disclaimer