A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv982193



Internal ID18617388
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr9:6291751..6292751hg38UCSC Ensembl
Innerchr9:6291751..6292751hg19UCSC Ensembl
Innerchr9:6281751..6282751hg18UCSC Ensembl
Cytoband9p24.1
Allele length
AssemblyAllele length
hg381001
hg191001
hg181001
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv2521351, nssv2521350, nssv2521346, nssv2521354, nssv2521345, nssv2521347, nssv2521348, nssv2521352, nssv2521353, nssv2521349
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)nsv982193
Frequency
Sample Size10
Observed Gain10
Observed Loss0
Observed Complex0
Frequencyn/a


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