A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv1871892



Internal ID17779594
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr11:96759..113009hg38UCSC Ensembl
Innerchr11:96759..113009hg19UCSC Ensembl
Innerchr11:86759..103009hg18UCSC Ensembl
Cytoband11p15.5
Allele length
AssemblyAllele length
hg3816251
hg1916251
hg1816251
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag1
Merged StatusS
Merged Variantsnsv971969
Supporting Variants
SamplesHGDP00665
Known Genes
MethodSequencing
Analysislineage specific fixed duplications
PlatformNot reported
Commentslineage specific duplication - fixed_Ggod-Ggog-Gbeg-Ptrs-Ptrt-Ptre-Ptrv-Ppa-Hsa-Hde
ReferenceSudmant_et_al_2013
Pubmed ID23825009
Accession Number(s)nssv1871892
Frequency
Sample Size10
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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