A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv975963



Internal ID18611170
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr11:89552794..89608165hg38UCSC Ensembl
Innerchr11:89285962..89341333hg19UCSC Ensembl
Innerchr11:88925610..88980981hg18UCSC Ensembl
Cytoband11q14.3
Allele length
AssemblyAllele length
hg3855372
hg1955372
hg1855372
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv1900286, nssv1900280, nssv1900285, nssv1900281, nssv1900278, nssv1900287, nssv1900284, nssv1900282, nssv1900279, nssv1900283
SamplesHGDP01284, HGDP00665, HGDP00998, HGDP00521, HGDP00778, HGDP01307, HGDP00542, HGDP01029, HGDP00456, HGDP00927
Known GenesNOX4
MethodSequencing
Analysislineage specific fixed duplications
PlatformNot reported
Comments
ReferenceSudmant_et_al_2013
Pubmed ID23825009
Accession Number(s)nsv975963
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