A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv975167



Internal ID18610375
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr11:38743674..38759194hg38UCSC Ensembl
Innerchr11:38765224..38780744hg19UCSC Ensembl
Innerchr11:38721800..38737320hg18UCSC Ensembl
Cytoband11p12
Allele length
AssemblyAllele length
hg3815521
hg1915521
hg1815521
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv1880912, nssv1880916, nssv1880917, nssv1880914, nssv1880915, nssv1880919, nssv1880911, nssv1880918, nssv1880913, nssv1880920
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)nsv975167
Frequency
Sample Size10
Observed Gain10
Observed Loss0
Observed Complex0
Frequencyn/a


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