A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv968702



Internal ID18603930
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr9:68220553..68238951hg38UCSC Ensembl
Innerchr9:70835469..70853867hg19UCSC Ensembl
Innerchr9:70025069..70043687hg18UCSC Ensembl
Cytoband9q13
Allele length
AssemblyAllele length
hg3818399
hg1918399
hg1818619
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv2551072, nssv2551064, nssv2551065, nssv2551068, nssv2551067, nssv2551069, nssv2551070, nssv2551071, nssv2551073, nssv2551066
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)nsv968702
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