A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv983000



Internal ID18271508
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr11:32590760..32592718hg38UCSC Ensembl
Innerchr11:32612306..32614264hg19UCSC Ensembl
Innerchr11:32568882..32570840hg18UCSC Ensembl
Cytoband11p13
Allele length
AssemblyAllele length
hg381959
hg191959
hg181959
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv1881114, nssv1881113, nssv1881119, nssv1881121, nssv1881117, nssv1881118, nssv1881115, nssv1881120, nssv1881112, nssv1881116
SamplesHGDP01284, HGDP00665, HGDP00998, HGDP00521, HGDP00778, HGDP01307, HGDP00542, HGDP01029, HGDP00456, HGDP00927
Known GenesEIF3M
MethodSequencing
Analysislineage specific fixed duplications
PlatformNot reported
Comments
ReferenceSudmant_et_al_2013
Pubmed ID23825009
Accession Number(s)nsv983000
Frequency
Sample Size10
Observed Gain10
Observed Loss0
Observed Complex0
Frequencyn/a


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