A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv964083



Internal ID18599321
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr4:111551400..111553029hg38UCSC Ensembl
Innerchr4:112472556..112474185hg19UCSC Ensembl
Innerchr4:112692005..112693634hg18UCSC Ensembl
Cytoband4q25
Allele length
AssemblyAllele length
hg381630
hg191630
hg181630
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv2332405, nssv2332403, nssv2332402, nssv2332401, nssv2332407, nssv2332409, nssv2332406, nssv2332404, nssv2332408, nssv2332400
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)nsv964083
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