A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv974534



Internal ID18609745
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr15:25579790..25588995hg38UCSC Ensembl
Innerchr15:25824937..25834142hg19UCSC Ensembl
Innerchr15:23376030..23385235hg18UCSC Ensembl
Cytoband15q12
Allele length
AssemblyAllele length
hg389206
hg199206
hg189206
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv2012862, nssv2012854, nssv2012856, nssv2012858, nssv2012861, nssv2012860, nssv2012859, nssv2012857, nssv2012855, nssv2012853
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)nsv974534
Frequency
Sample Size10
Observed Gain10
Observed Loss0
Observed Complex0
Frequencyn/a


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