A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv1877076



Internal ID17779856
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr11:16481270..16484491hg38UCSC Ensembl
Innerchr11:16502817..16506038hg19UCSC Ensembl
Innerchr11:16459393..16462614hg18UCSC Ensembl
Cytoband11p15.1
Allele length
AssemblyAllele length
hg383222
hg193222
hg183222
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv982987
Supporting Variants
SamplesHGDP00665
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)nssv1877076
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