A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv1898745



Internal ID17776940
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr11:86195689..86196905hg38UCSC Ensembl
Innerchr11:85906731..85907947hg19UCSC Ensembl
Innerchr11:85584379..85585595hg18UCSC Ensembl
Cytoband11q14.2
Allele length
AssemblyAllele length
hg381217
hg191217
hg181217
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv975958
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)nssv1898745
Frequency
Sample Size10
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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