A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv1893894



Internal ID17871058
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr11:65954093..65958375hg38UCSC Ensembl
Innerchr11:65721564..65725846hg19UCSC Ensembl
Innerchr11:65478140..65482422hg18UCSC Ensembl
Cytoband11q13.1
Allele length
AssemblyAllele length
hg384283
hg194283
hg184283
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv983036
Supporting Variants
SamplesHGDP01284
Known GenesTSGA10IP
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)nssv1893894
Frequency
Sample Size10
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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