A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv975146



Internal ID18610354
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr11:6026899..6027618hg38UCSC Ensembl
Innerchr11:6048129..6048848hg19UCSC Ensembl
Innerchr11:6004705..6005424hg18UCSC Ensembl
Cytoband11p15.4
Allele length
AssemblyAllele length
hg38720
hg19720
hg18720
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv1874477, nssv1874476, nssv1874471, nssv1874473, nssv1874469, nssv1874468, nssv1874474, nssv1874475, nssv1874472, nssv1874470
SamplesHGDP01284, HGDP00665, HGDP00998, HGDP00521, HGDP00778, HGDP01307, HGDP00542, HGDP01029, HGDP00456, HGDP00927
Known GenesOR56A1
MethodSequencing
Analysislineage specific fixed duplications
PlatformNot reported
Comments
ReferenceSudmant_et_al_2013
Pubmed ID23825009
Accession Number(s)nsv975146
Frequency
Sample Size10
Observed Gain10
Observed Loss0
Observed Complex0
Frequencyn/a


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