A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv983859



Internal ID18619051
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr14:103373163..103378008hg38UCSC Ensembl
Innerchr14:103839500..103844345hg19UCSC Ensembl
Innerchr14:102909253..102914098hg18UCSC Ensembl
Cytoband14q32.32
Allele length
AssemblyAllele length
hg384846
hg194846
hg184846
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv1997835, nssv1997831, nssv1997830, nssv1997836, nssv1997833, nssv1997829, nssv1997832, nssv1997837, nssv1997838, nssv1997834
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)nsv983859
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