A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv975223



Internal ID18610431
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr11:105033749..105034880hg38UCSC Ensembl
Innerchr11:104904476..104905607hg19UCSC Ensembl
Innerchr11:104409686..104410817hg18UCSC Ensembl
Cytoband11q22.3
Allele length
AssemblyAllele length
hg381132
hg191132
hg181132
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv1901590, nssv1901593, nssv1901594, nssv1901595, nssv1901591, nssv1901589, nssv1901587, nssv1901592, nssv1901586, nssv1901588
SamplesHGDP01284, HGDP00665, HGDP00998, HGDP00521, HGDP00778, HGDP01307, HGDP00542, HGDP01029, HGDP00456, HGDP00927
Known GenesCASP1
MethodSequencing
Analysislineage specific fixed duplications
PlatformNot reported
Comments
ReferenceSudmant_et_al_2013
Pubmed ID23825009
Accession Number(s)nsv975223
Frequency
Sample Size10
Observed Gain10
Observed Loss0
Observed Complex0
Frequencyn/a


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