A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv982308



Internal ID18617503
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr9:78178897..78188733hg38UCSC Ensembl
Innerchr9:80793813..80803649hg19UCSC Ensembl
Innerchr9:79983633..79993469hg18UCSC Ensembl
Cytoband9q21.2
Allele length
AssemblyAllele length
hg389837
hg199837
hg189837
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv2553092, nssv2553089, nssv2553094, nssv2553085, nssv2553086, nssv2553087, nssv2553093, nssv2553091, nssv2553088, nssv2553090
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)nsv982308
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