A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv983025



Internal ID18618219
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr11:57574247..57577057hg38UCSC Ensembl
Innerchr11:57341720..57344530hg19UCSC Ensembl
Innerchr11:57098296..57101106hg18UCSC Ensembl
Cytoband11q12.1
Allele length
AssemblyAllele length
hg382811
hg192811
hg182811
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv1890557, nssv1890563, nssv1890562, nssv1890558, nssv1890559, nssv1890554, nssv1890561, nssv1890555, nssv1890556, nssv1890560
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)nsv983025
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