A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv976355



Internal ID18611561
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr14:75595308..75596136hg38UCSC Ensembl
Innerchr14:76061651..76062479hg19UCSC Ensembl
Innerchr14:75131404..75132232hg18UCSC Ensembl
Cytoband14q24.3
Allele length
AssemblyAllele length
hg38829
hg19829
hg18829
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv1991891, nssv1991888, nssv1991889, nssv1991887, nssv1991886, nssv1991885, nssv1991894, nssv1991890, nssv1991893, nssv1991892
SamplesHGDP01284, HGDP00665, HGDP00998, HGDP00521, HGDP00778, HGDP01307, HGDP00542, HGDP01029, HGDP00456, HGDP00927
Known GenesFLVCR2
MethodSequencing
Analysislineage specific fixed duplications
PlatformNot reported
Comments
ReferenceSudmant_et_al_2013
Pubmed ID23825009
Accession Number(s)nsv976355
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