A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv982298



Internal ID18617493
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr9:65737118..65768709hg38UCSC Ensembl
Innerchr9:70397336..70428927hg19UCSC Ensembl
Innerchr9:69637156..69668747hg18UCSC Ensembl
Cytoband9q12
Allele length
AssemblyAllele length
hg3831592
hg1931592
hg1831592
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv2551303, nssv2551298, nssv2551302, nssv2551297, nssv2551299, nssv2551294, nssv2551295, nssv2551296, nssv2551301, nssv2551300
SamplesHGDP01284, HGDP00665, HGDP00998, HGDP00521, HGDP00778, HGDP01307, HGDP00542, HGDP01029, HGDP00456, HGDP00927
Known GenesFOXD4L2, FOXD4L4
MethodSequencing
Analysislineage specific fixed duplications
PlatformNot reported
Comments
ReferenceSudmant_et_al_2013
Pubmed ID23825009
Accession Number(s)nsv982298
Frequency
Sample Size10
Observed Gain10
Observed Loss0
Observed Complex0
Frequencyn/a


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