A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv982992



Internal ID18618186
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr11:18665125..18666125hg38UCSC Ensembl
Innerchr11:18686672..18687672hg19UCSC Ensembl
Innerchr11:18643248..18644248hg18UCSC Ensembl
Cytoband11p15.1
Allele length
AssemblyAllele length
hg381001
hg191001
hg181001
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv1878355, nssv1878358, nssv1878353, nssv1878352, nssv1878356, nssv1878351, nssv1878359, nssv1878360, nssv1878357, nssv1878354
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)nsv982992
Frequency
Sample Size10
Observed Gain10
Observed Loss0
Observed Complex0
Frequencyn/a


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