A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv1905184



Internal ID17796913
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr11:110783879..110791394hg38UCSC Ensembl
Innerchr11:110654602..110662117hg19UCSC Ensembl
Innerchr11:110159812..110167327hg18UCSC Ensembl
Cytoband11q23.1
Allele length
AssemblyAllele length
hg387516
hg197516
hg187516
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv983061
Supporting Variants
SamplesHGDP00778
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)nssv1905184
Frequency
Sample Size10
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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