A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv983057



Internal ID18618251
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr11:100666016..100667328hg38UCSC Ensembl
Innerchr11:100536747..100538059hg19UCSC Ensembl
Innerchr11:100041957..100043269hg18UCSC Ensembl
Cytoband11q22.1
Allele length
AssemblyAllele length
hg381313
hg191313
hg181313
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv1902276, nssv1902272, nssv1902270, nssv1902274, nssv1902271, nssv1902278, nssv1902277, nssv1902273, nssv1902275, nssv1902279
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)nsv983057
Frequency
Sample Size10
Observed Gain10
Observed Loss0
Observed Complex0
Frequencyn/a


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