A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv975898



Internal ID18611105
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr11:31274229..31283848hg38UCSC Ensembl
Innerchr11:31295776..31305395hg19UCSC Ensembl
Innerchr11:31252352..31261971hg18UCSC Ensembl
Cytoband11p13
Allele length
AssemblyAllele length
hg389620
hg199620
hg189620
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv1880133, nssv1880128, nssv1880129, nssv1880131, nssv1880132, nssv1880127, nssv1880130, nssv1880126, nssv1880135, nssv1880134
SamplesHGDP01284, HGDP00665, HGDP00998, HGDP00521, HGDP00778, HGDP01307, HGDP00542, HGDP01029, HGDP00456, HGDP00927
Known GenesDCDC1
MethodSequencing
Analysislineage specific fixed duplications
PlatformNot reported
Comments
ReferenceSudmant_et_al_2013
Pubmed ID23825009
Accession Number(s)nsv975898
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