A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv976356



Internal ID18611562
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr14:76886304..76886899hg38UCSC Ensembl
Innerchr14:77352647..77353242hg19UCSC Ensembl
Innerchr14:76422400..76422995hg18UCSC Ensembl
Cytoband14q24.3
Allele length
AssemblyAllele length
hg38596
hg19596
hg18596
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv1992873, nssv1992876, nssv1992877, nssv1992872, nssv1992880, nssv1992879, nssv1992871, nssv1992875, nssv1992878, nssv1992874
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)nsv976356
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