A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv947927



Internal ID18248087
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr10:46650504..46651744hg38UCSC Ensembl
Innerchr10:46897873..46899113hg19UCSC Ensembl
Innerchr10:46317879..46319119hg18UCSC Ensembl
Cytoband10q11.22
Allele length
AssemblyAllele length
hg381241
hg191241
hg181241
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv1845838, nssv1845840, nssv1845842, nssv1845843, nssv1845839, nssv1845834, nssv1845841, nssv1845835, nssv1845836, nssv1845837
SamplesHGDP00927, HGDP00778, HGDP00542, HGDP01029, HGDP01284, HGDP00521, HGDP00998, HGDP00456, HGDP01307, HGDP00665
Known GenesFAM35BP
MethodSequencing
Analysislineage specific fixed duplications
PlatformNot reported
Comments
ReferenceSudmant_et_al_2013
Pubmed ID23825009
Accession Number(s)nsv947927
Frequency
Sample Size10
Observed Gain10
Observed Loss0
Observed Complex0
Frequencyn/a


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