A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv1882007



Internal ID17846856
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr11:39161388..39162408hg38UCSC Ensembl
Innerchr11:39182938..39183958hg19UCSC Ensembl
Innerchr11:39139514..39140534hg18UCSC Ensembl
Cytoband11p12
Allele length
AssemblyAllele length
hg381021
hg191021
hg181021
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv983004
Supporting Variants
SamplesHGDP01029
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)nssv1882007
Frequency
Sample Size10
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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