A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv972015



Internal ID18260545
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr11:49165970..49219167hg38UCSC Ensembl
Innerchr11:49187522..49240719hg19UCSC Ensembl
Innerchr11:49144098..49197295hg18UCSC Ensembl
Cytoband11p11.12
Allele length
AssemblyAllele length
hg3853198
hg1953198
hg1853198
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv1885926, nssv1885920, nssv1885922, nssv1885923, nssv1885919, nssv1885927, nssv1885918, nssv1885925, nssv1885924, nssv1885921
SamplesHGDP00927, HGDP00778, HGDP00542, HGDP01029, HGDP01284, HGDP00521, HGDP00998, HGDP00456, HGDP01307, HGDP00665
Known GenesFOLH1
MethodSequencing
Analysislineage specific fixed duplications
PlatformNot reported
Comments
ReferenceSudmant_et_al_2013
Pubmed ID23825009
Accession Number(s)nsv972015
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