A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv975150



Internal ID18610358
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr11:10153033..10160695hg38UCSC Ensembl
Innerchr11:10174580..10182242hg19UCSC Ensembl
Innerchr11:10131156..10138818hg18UCSC Ensembl
Cytoband11p15.4
Allele length
AssemblyAllele length
hg387663
hg197663
hg187663
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv1875969, nssv1875965, nssv1875966, nssv1875972, nssv1875971, nssv1875967, nssv1875970, nssv1875968, nssv1875964, nssv1875963
SamplesHGDP01284, HGDP00665, HGDP00998, HGDP00521, HGDP00778, HGDP01307, HGDP00542, HGDP01029, HGDP00456, HGDP00927
Known GenesSBF2
MethodSequencing
Analysislineage specific fixed duplications
PlatformNot reported
Comments
ReferenceSudmant_et_al_2013
Pubmed ID23825009
Accession Number(s)nsv975150
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