A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv975211



Internal ID18610419
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr11:87477897..87490331hg38UCSC Ensembl
Innerchr11:87188939..87201373hg19UCSC Ensembl
Innerchr11:86866587..86879021hg18UCSC Ensembl
Cytoband11q14.2
Allele length
AssemblyAllele length
hg3812435
hg1912435
hg1812435
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv1898348, nssv1898351, nssv1898350, nssv1898345, nssv1898349, nssv1898346, nssv1898347, nssv1898352, nssv1898353, nssv1898344
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)nsv975211
Frequency
Sample Size10
Observed Gain10
Observed Loss0
Observed Complex0
Frequencyn/a


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