A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv975954



Internal ID18264475
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr11:77889869..77906857hg38UCSC Ensembl
Innerchr11:77600915..77617903hg19UCSC Ensembl
Innerchr11:77278563..77295551hg18UCSC Ensembl
Cytoband11q14.1
Allele length
AssemblyAllele length
hg3816989
hg1916989
hg1816989
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv1897362, nssv1897356, nssv1897365, nssv1897359, nssv1897364, nssv1897358, nssv1897361, nssv1897363, nssv1897357, nssv1897360
SamplesHGDP01284, HGDP00665, HGDP00998, HGDP00521, HGDP00778, HGDP01307, HGDP00542, HGDP01029, HGDP00456, HGDP00927
Known GenesINTS4
MethodSequencing
Analysislineage specific fixed duplications
PlatformNot reported
Comments
ReferenceSudmant_et_al_2013
Pubmed ID23825009
Accession Number(s)nsv975954
Frequency
Sample Size10
Observed Gain10
Observed Loss0
Observed Complex0
Frequencyn/a


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