A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv975941



Internal ID18264462
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr11:63758748..63759972hg38UCSC Ensembl
Innerchr11:63526220..63527444hg19UCSC Ensembl
Innerchr11:63282796..63284020hg18UCSC Ensembl
Cytoband11q13.1
Allele length
AssemblyAllele length
hg381225
hg191225
hg181225
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv1893400, nssv1893401, nssv1893403, nssv1893404, nssv1893398, nssv1893399, nssv1893396, nssv1893402, nssv1893405, nssv1893397
SamplesHGDP01284, HGDP00665, HGDP00998, HGDP00521, HGDP00778, HGDP01307, HGDP00542, HGDP01029, HGDP00456, HGDP00927
Known GenesC11orf95, RTN3
MethodSequencing
Analysislineage specific fixed duplications
PlatformNot reported
Comments
ReferenceSudmant_et_al_2013
Pubmed ID23825009
Accession Number(s)nsv975941
Frequency
Sample Size10
Observed Gain10
Observed Loss0
Observed Complex0
Frequencyn/a


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