A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv983056



Internal ID18618250
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr11:95049280..95050920hg38UCSC Ensembl
Innerchr11:94782444..94784084hg19UCSC Ensembl
Innerchr11:94422092..94423732hg18UCSC Ensembl
Cytoband11q21
Allele length
AssemblyAllele length
hg381641
hg191641
hg181641
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv1903203, nssv1903207, nssv1903205, nssv1903206, nssv1903202, nssv1903200, nssv1903208, nssv1903204, nssv1903201, nssv1903209
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)nsv983056
Frequency
Sample Size10
Observed Gain10
Observed Loss0
Observed Complex0
Frequencyn/a


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