A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv1896901



Internal ID17761401
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr11:83213022..83224238hg38UCSC Ensembl
Innerchr11:82924064..82935280hg19UCSC Ensembl
Innerchr11:82601712..82612928hg18UCSC Ensembl
Cytoband11q14.1
Allele length
AssemblyAllele length
hg3811217
hg1911217
hg1811217
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv972051
Supporting Variants
SamplesHGDP00542
Known GenesANKRD42
MethodSequencing
Analysislineage specific fixed duplications
PlatformNot reported
Commentslineage specific duplication - fixed_Pab-Ppy-Ggod-Ggog-Gbeg-Ptrs-Ptrt-Ptre-Ptrv-Ppa-Hsa-Hde
ReferenceSudmant_et_al_2013
Pubmed ID23825009
Accession Number(s)nssv1896901
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