A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv983004



Internal ID18618198
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr11:39161388..39162408hg38UCSC Ensembl
Innerchr11:39182938..39183958hg19UCSC Ensembl
Innerchr11:39139514..39140534hg18UCSC Ensembl
Cytoband11p12
Allele length
AssemblyAllele length
hg381021
hg191021
hg181021
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv1882000, nssv1882006, nssv1882005, nssv1882001, nssv1882002, nssv1882004, nssv1882003, nssv1882009, nssv1882007, nssv1882008
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)nsv983004
Frequency
Sample Size10
Observed Gain10
Observed Loss0
Observed Complex0
Frequencyn/a


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