A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv982978



Internal ID18618172
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr11:5993042..5995541hg38UCSC Ensembl
Innerchr11:6014272..6016771hg19UCSC Ensembl
Innerchr11:5970848..5973347hg18UCSC Ensembl
Cytoband11p15.4
Allele length
AssemblyAllele length
hg382500
hg192500
hg182500
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv1874376, nssv1874372, nssv1874377, nssv1874374, nssv1874379, nssv1874375, nssv1874380, nssv1874373, nssv1874378, nssv1873579
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)nsv982978
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