A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv1898281



Internal ID17813870
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr11:82798430..82807047hg38UCSC Ensembl
Innerchr11:82509472..82518089hg19UCSC Ensembl
Innerchr11:82187120..82195737hg18UCSC Ensembl
Cytoband11q14.1
Allele length
AssemblyAllele length
hg388618
hg198618
hg188618
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv972049
Supporting Variants
SamplesHGDP00927
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)nssv1898281
Frequency
Sample Size10
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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