A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv975959



Internal ID18611166
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr11:86823683..86857877hg38UCSC Ensembl
Innerchr11:86534725..86568919hg19UCSC Ensembl
Innerchr11:86212373..86246567hg18UCSC Ensembl
Cytoband11q14.2
Allele length
AssemblyAllele length
hg3834195
hg1934195
hg1834195
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv1897103, nssv1897100, nssv1897095, nssv1897098, nssv1897096, nssv1897099, nssv1897101, nssv1897094, nssv1897102, nssv1897097
SamplesHGDP01284, HGDP00665, HGDP00998, HGDP00521, HGDP00778, HGDP01307, HGDP00542, HGDP01029, HGDP00456, HGDP00927
Known GenesOR7E2P
MethodSequencing
Analysislineage specific fixed duplications
PlatformNot reported
Comments
ReferenceSudmant_et_al_2013
Pubmed ID23825009
Accession Number(s)nsv975959
Frequency
Sample Size10
Observed Gain10
Observed Loss0
Observed Complex0
Frequencyn/a


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