A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv975878



Internal ID18264399
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr11:6683474..6694742hg38UCSC Ensembl
Innerchr11:6704705..6715973hg19UCSC Ensembl
Innerchr11:6661281..6672549hg18UCSC Ensembl
Cytoband11p15.4
Allele length
AssemblyAllele length
hg3811269
hg1911269
hg1811269
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv1875912, nssv1875921, nssv1875916, nssv1875920, nssv1875913, nssv1875917, nssv1875918, nssv1875914, nssv1875915, nssv1875919
SamplesHGDP01284, HGDP00665, HGDP00998, HGDP00521, HGDP00778, HGDP01307, HGDP00542, HGDP01029, HGDP00456, HGDP00927
Known Genes
MethodSequencing
Analysislineage specific fixed duplications
PlatformNot reported
Comments
ReferenceSudmant_et_al_2013
Pubmed ID23825009
Accession Number(s)nsv975878
Frequency
Sample Size10
Observed Gain10
Observed Loss0
Observed Complex0
Frequencyn/a


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