A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv975960



Internal ID18611167
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr11:87024744..87029053hg38UCSC Ensembl
Innerchr11:86735786..86740095hg19UCSC Ensembl
Innerchr11:86413434..86417743hg18UCSC Ensembl
Cytoband11q14.2
Allele length
AssemblyAllele length
hg384310
hg194310
hg184310
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv1897198, nssv1897195, nssv1897192, nssv1897199, nssv1897191, nssv1897194, nssv1897193, nssv1897197, nssv1897200, nssv1897196
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)nsv975960
Frequency
Sample Size10
Observed Gain10
Observed Loss0
Observed Complex0
Frequencyn/a


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