A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv975198



Internal ID18263720
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr11:69303056..69304959hg38UCSC Ensembl
Innerchr11:69070523..69072426hg19UCSC Ensembl
Innerchr11:68827099..68829002hg18UCSC Ensembl
Cytoband11q13.2
Allele length
AssemblyAllele length
hg381904
hg191904
hg181904
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv1894734, nssv1894738, nssv1894735, nssv1894736, nssv1894733, nssv1894737, nssv1894732, nssv1894731, nssv1894740, nssv1894739
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)nsv975198
Frequency
Sample Size10
Observed Gain10
Observed Loss0
Observed Complex0
Frequencyn/a


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