A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv975843



Internal ID18611050
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr11:54655724..54660623hg38UCSC Ensembl
Innerchr11:51458657..51463556hg19UCSC Ensembl
Innerchr11:51315233..51320132hg18UCSC Ensembl
Cytoband11p11.12
Allele length
AssemblyAllele length
hg384900
hg194900
hg184900
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv1888215, nssv1888222, nssv1888219, nssv1888218, nssv1888214, nssv1888221, nssv1888220, nssv1888217, nssv1888216, nssv1888213
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)nsv975843
Frequency
Sample Size10
Observed Gain10
Observed Loss0
Observed Complex0
Frequencyn/a


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