A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv983053



Internal ID18618247
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr11:93051586..93052736hg38UCSC Ensembl
Innerchr11:92784752..92785902hg19UCSC Ensembl
Innerchr11:92424400..92425550hg18UCSC Ensembl
Cytoband11q14.3
Allele length
AssemblyAllele length
hg381151
hg191151
hg181151
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv1901246, nssv1901251, nssv1901253, nssv1901248, nssv1901255, nssv1901247, nssv1901254, nssv1901252, nssv1901250, nssv1901249
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)nsv983053
Frequency
Sample Size10
Observed Gain10
Observed Loss0
Observed Complex0
Frequencyn/a


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