A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv966299



Internal ID18254843
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr4:98879204..98881274hg38UCSC Ensembl
Innerchr4:99800355..99802425hg19UCSC Ensembl
Innerchr4:100019378..100021448hg18UCSC Ensembl
Cytoband4q23
Allele length
AssemblyAllele length
hg382071
hg192071
hg182071
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv2326892, nssv2326887, nssv2326889, nssv2326893, nssv2326895, nssv2326891, nssv2326894, nssv2326888, nssv2326890, nssv2326886
SamplesHGDP01284, HGDP00665, HGDP00998, HGDP00521, HGDP00778, HGDP01307, HGDP00542, HGDP01029, HGDP00456, HGDP00927
Known GenesEIF4E
MethodSequencing
Analysislineage specific fixed duplications
PlatformNot reported
Comments
ReferenceSudmant_et_al_2013
Pubmed ID23825009
Accession Number(s)nsv966299
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