A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv972065



Internal ID18607281
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr11:103045084..103045935hg38UCSC Ensembl
Innerchr11:102915813..102916664hg19UCSC Ensembl
Innerchr11:102421023..102421874hg18UCSC Ensembl
Cytoband11q22.3
Allele length
AssemblyAllele length
hg38852
hg19852
hg18852
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv1903452, nssv1903459, nssv1903456, nssv1903458, nssv1903451, nssv1903450, nssv1903453, nssv1903457, nssv1903454, nssv1903455
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)nsv972065
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