A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv982265



Internal ID18617460
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr9:67608563..67622659hg38UCSC Ensembl
Innerchr9:46266431..46281131hg19UCSC Ensembl
Innerchr9:46156284..46171127hg18UCSC Ensembl
Cytoband9p11.2
Allele length
AssemblyAllele length
hg3814097
hg1914701
hg1814844
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv2543220, nssv2543218, nssv2543221, nssv2543216, nssv2543219, nssv2543214, nssv2543215, nssv2543212, nssv2543217, nssv2543213
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)nsv982265
Frequency
Sample Size10
Observed Gain10
Observed Loss0
Observed Complex0
Frequencyn/a


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