A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv1890795



Internal ID17842886
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr11:58203128..58215640hg38UCSC Ensembl
Innerchr11:57970600..57983112hg19UCSC Ensembl
Innerchr11:57727176..57739688hg18UCSC Ensembl
Cytoband11q12.1
Allele length
AssemblyAllele length
hg3812513
hg1912513
hg1812513
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv972033
Supporting Variants
SamplesHGDP01029
Known GenesOR1S1, OR1S2
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)nssv1890795
Frequency
Sample Size10
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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