A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv965895



Internal ID18601125
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr20:59358494..59359351hg38UCSC Ensembl
Innerchr20:57933549..57934406hg19UCSC Ensembl
Innerchr20:57366944..57367801hg18UCSC Ensembl
Cytoband20q13.32
Allele length
AssemblyAllele length
hg38858
hg19858
hg18858
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv2241472, nssv2241468, nssv2241473, nssv2241475, nssv2240674, nssv2241471, nssv2240675, nssv2241474, nssv2241470, nssv2241469
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)nsv965895
Frequency
Sample Size10
Observed Gain10
Observed Loss0
Observed Complex0
Frequencyn/a


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