A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv947928



Internal ID18248088
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr10:46583673..46650504hg38UCSC Ensembl
Innerchr10:46899113..46965944hg19UCSC Ensembl
Innerchr10:46319119..46385950hg18UCSC Ensembl
Cytoband10q11.22
Allele length
AssemblyAllele length
hg3866832
hg1966832
hg1866832
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv1844056, nssv1844055, nssv1844058, nssv1844052, nssv1844054, nssv1844059, nssv1844060, nssv1844061, nssv1844057, nssv1844053
SamplesHGDP00927, HGDP00778, HGDP00542, HGDP01029, HGDP01284, HGDP00521, HGDP00998, HGDP00456, HGDP01307, HGDP00665
Known GenesFAM35BP, SYT15
MethodSequencing
Analysislineage specific fixed duplications
PlatformNot reported
Comments
ReferenceSudmant_et_al_2013
Pubmed ID23825009
Accession Number(s)nsv947928
Frequency
Sample Size10
Observed Gain10
Observed Loss0
Observed Complex0
Frequencyn/a


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