A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv1907355



Internal ID17829531
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr11:122960614..122961114hg38UCSC Ensembl
Innerchr11:122831322..122831822hg19UCSC Ensembl
Innerchr11:122336532..122337032hg18UCSC Ensembl
Cytoband11q24.1
Allele length
AssemblyAllele length
hg38501
hg19501
hg18501
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv975234
Supporting Variants
SamplesHGDP00998
Known Genes
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)nssv1907355
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