A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv982254



Internal ID18617449
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr9:42554393..42578202hg38UCSC Ensembl
Innerchr9:44392905..44416726hg19UCSC Ensembl
Innerchr9:44332901..44356722hg18UCSC Ensembl
Cytoband9p11.2
Allele length
AssemblyAllele length
hg3823810
hg1923822
hg1823822
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv89n82
Supporting Variantsnssv2540334, nssv2540342, nssv2540338, nssv2540343, nssv2540335, nssv2540340, nssv2540337, nssv2540341, nssv2540336, nssv2540339
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)nsv982254
Frequency
Sample Size10
Observed Gain10
Observed Loss0
Observed Complex0
Frequencyn/a


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