A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv981589



Internal ID18270100
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr7:138479101..138492710hg38UCSC Ensembl
Innerchr7:138163846..138177455hg19UCSC Ensembl
Innerchr7:137814386..137827995hg18UCSC Ensembl
Cytoband7q33
Allele length
AssemblyAllele length
hg3813610
hg1913610
hg1813610
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv2479638, nssv2479639, nssv2479640, nssv2479644, nssv2479645, nssv2479643, nssv2479642, nssv2479646, nssv2479641, nssv2479647
SamplesHGDP00927, HGDP00778, HGDP00542, HGDP01029, HGDP01284, HGDP00521, HGDP00998, HGDP00456, HGDP01307, HGDP00665
Known GenesTRIM24
MethodSequencing
Analysislineage specific fixed duplications
PlatformNot reported
Comments
ReferenceSudmant_et_al_2013
Pubmed ID23825009
Accession Number(s)nsv981589
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