A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv975886



Internal ID18264407
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr11:13684801..13686394hg38UCSC Ensembl
Innerchr11:13706348..13707941hg19UCSC Ensembl
Innerchr11:13662924..13664517hg18UCSC Ensembl
Cytoband11p15.2
Allele length
AssemblyAllele length
hg381594
hg191594
hg181594
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv1877657, nssv1877653, nssv1877654, nssv1877650, nssv1877652, nssv1877656, nssv1877651, nssv1877649, nssv1877655, nssv1877648
SamplesHGDP00927, HGDP00778, HGDP00542, HGDP01029, HGDP01284, HGDP00521, HGDP00998, HGDP00456, HGDP01307, HGDP00665
Known GenesFAR1
MethodSequencing
Analysislineage specific fixed duplications
PlatformNot reported
Comments
ReferenceSudmant_et_al_2013
Pubmed ID23825009
Accession Number(s)nsv975886
Frequency
Sample Size10
Observed Gain10
Observed Loss0
Observed Complex0
Frequencyn/a


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