A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv982998



Internal ID18271506
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr11:27581649..27582250hg38UCSC Ensembl
Innerchr11:27603196..27603797hg19UCSC Ensembl
Innerchr11:27559772..27560373hg18UCSC Ensembl
Cytoband11p14.1
Allele length
AssemblyAllele length
hg38602
hg19602
hg18602
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv1880655, nssv1878026, nssv1878027, nssv1880652, nssv1880654, nssv1878025, nssv1880658, nssv1880657, nssv1880656, nssv1880653
SamplesHGDP01284, HGDP00665, HGDP00998, HGDP00521, HGDP00778, HGDP01307, HGDP00542, HGDP01029, HGDP00456, HGDP00927
Known GenesBDNF-AS
MethodSequencing
Analysislineage specific fixed duplications
PlatformNot reported
Comments
ReferenceSudmant_et_al_2013
Pubmed ID23825009
Accession Number(s)nsv982998
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