A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv975940



Internal ID18264461
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr11:63541758..63543741hg38UCSC Ensembl
Innerchr11:63309230..63311213hg19UCSC Ensembl
Innerchr11:63065806..63067789hg18UCSC Ensembl
Cytoband11q12.3
Allele length
AssemblyAllele length
hg381984
hg191984
hg181984
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv1892507, nssv1892516, nssv1892510, nssv1892514, nssv1892515, nssv1892508, nssv1892511, nssv1892513, nssv1892512, nssv1892509
SamplesHGDP00927, HGDP00778, HGDP00542, HGDP01029, HGDP01284, HGDP00521, HGDP00998, HGDP00456, HGDP01307, HGDP00665
Known GenesMIR3680-1, MIR3680-2, RARRES3
MethodSequencing
Analysislineage specific fixed duplications
PlatformNot reported
Comments
ReferenceSudmant_et_al_2013
Pubmed ID23825009
Accession Number(s)nsv975940
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