A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv975210



Internal ID18610418
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr11:86294845..86295345hg38UCSC Ensembl
Innerchr11:86005887..86006387hg19UCSC Ensembl
Innerchr11:85683535..85684035hg18UCSC Ensembl
Cytoband11q14.2
Allele length
AssemblyAllele length
hg38501
hg19501
hg18501
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv1897000, nssv1897004, nssv1897001, nssv1896997, nssv1896999, nssv1897005, nssv1897006, nssv1897002, nssv1896998, nssv1897003
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)nsv975210
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