A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv983809



Internal ID18619001
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr14:27794584..27860661hg38UCSC Ensembl
Innerchr14:28263790..28329867hg19UCSC Ensembl
Innerchr14:27333630..27399707hg18UCSC Ensembl
Cytoband14q12
Allele length
AssemblyAllele length
hg3866078
hg1966078
hg1866078
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv1981629, nssv1981622, nssv1981627, nssv1981625, nssv1981628, nssv1981630, nssv1981623, nssv1981631, nssv1981624, nssv1981626
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)nsv983809
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