A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv983068



Internal ID18618262
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr11:119601955..119605859hg38UCSC Ensembl
Innerchr11:119472667..119476571hg19UCSC Ensembl
Innerchr11:118977877..118981781hg18UCSC Ensembl
Cytoband11q23.3
Allele length
AssemblyAllele length
hg383905
hg193905
hg183905
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv1906273, nssv1906272, nssv1906267, nssv1906265, nssv1906269, nssv1906268, nssv1906271, nssv1906274, nssv1906270, nssv1906266
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)nsv983068
Frequency
Sample Size10
Observed Gain10
Observed Loss0
Observed Complex0
Frequencyn/a


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