A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv983062



Internal ID18271570
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr11:112266989..112268325hg38UCSC Ensembl
Innerchr11:112137712..112139048hg19UCSC Ensembl
Innerchr11:111642922..111644258hg18UCSC Ensembl
Cytoband11q23.1
Allele length
AssemblyAllele length
hg381337
hg191337
hg181337
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv1905635, nssv1905634, nssv1905629, nssv1905632, nssv1905627, nssv1905633, nssv1905628, nssv1905630, nssv1905626, nssv1905631
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)nsv983062
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