A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv983035



Internal ID18618229
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr11:65727241..65762030hg38UCSC Ensembl
Innerchr11:65494712..65529501hg19UCSC Ensembl
Innerchr11:65251288..65286077hg18UCSC Ensembl
Cytoband11q13.1
Allele length
AssemblyAllele length
hg3834790
hg1934790
hg1834790
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv1893271, nssv1893264, nssv1893265, nssv1893263, nssv1893266, nssv1893269, nssv1893267, nssv1893270, nssv1893262, nssv1893268
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)nsv983035
Frequency
Sample Size10
Observed Gain10
Observed Loss0
Observed Complex0
Frequencyn/a


Hosted by The Centre for Applied Genomics
Grant support for DGV
Please read the usage disclaimer