A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv965185



Internal ID18600419
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr3:93814915..93844832hg38UCSC Ensembl
Innerchr3:93533759..93563676hg19UCSC Ensembl
Innerchr3:95016449..95046366hg18UCSC Ensembl
Cytoband3q11.1
Allele length
AssemblyAllele length
hg3829918
hg1929918
hg1829918
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv2289918, nssv2289916, nssv2289915, nssv2289914, nssv2289921, nssv2289917, nssv2289920, nssv2289922, nssv2289919, nssv2289913
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)nsv965185
Frequency
Sample Size10
Observed Gain10
Observed Loss0
Observed Complex0
Frequencyn/a


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