A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv972061



Internal ID18607277
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr11:92364655..92367727hg38UCSC Ensembl
Innerchr11:92097821..92100893hg19UCSC Ensembl
Innerchr11:91737469..91740541hg18UCSC Ensembl
Cytoband11q14.3
Allele length
AssemblyAllele length
hg383073
hg193073
hg183073
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv1901066, nssv1901064, nssv1901061, nssv1901065, nssv1901059, nssv1901062, nssv1901060, nssv1901063, nssv1901058, nssv1901067
SamplesHGDP01284, HGDP00665, HGDP00998, HGDP00521, HGDP00778, HGDP01307, HGDP00542, HGDP01029, HGDP00456, HGDP00927
Known GenesFAT3
MethodSequencing
Analysislineage specific fixed duplications
PlatformNot reported
Comments
ReferenceSudmant_et_al_2013
Pubmed ID23825009
Accession Number(s)nsv972061
Frequency
Sample Size10
Observed Gain10
Observed Loss0
Observed Complex0
Frequencyn/a


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