A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv981171



Internal ID18616370
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr6:108610688..108619291hg38UCSC Ensembl
Innerchr6:108931891..108940494hg19UCSC Ensembl
Innerchr6:109038584..109047187hg18UCSC Ensembl
Cytoband6q21
Allele length
AssemblyAllele length
hg388604
hg198604
hg188604
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv2420030, nssv2420036, nssv2420032, nssv2420033, nssv2420037, nssv2420034, nssv2420031, nssv2420039, nssv2420038, nssv2420035
SamplesHGDP01284, HGDP00665, HGDP00998, HGDP00521, HGDP00778, HGDP01307, HGDP00542, HGDP01029, HGDP00456, HGDP00927
Known GenesFOXO3
MethodSequencing
Analysislineage specific fixed duplications
PlatformNot reported
Comments
ReferenceSudmant_et_al_2013
Pubmed ID23825009
Accession Number(s)nsv981171
Frequency
Sample Size10
Observed Gain10
Observed Loss0
Observed Complex0
Frequencyn/a


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