A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv948141



Internal ID18594987
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr10:93206658..93212080hg38UCSC Ensembl
Innerchr10:94966415..94971837hg19UCSC Ensembl
Innerchr10:94956405..94961827hg18UCSC Ensembl
Cytoband10q23.33
Allele length
AssemblyAllele length
hg385423
hg195423
hg185423
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv1865519, nssv1865518, nssv1865511, nssv1865510, nssv1865517, nssv1865516, nssv1865512, nssv1865514, nssv1865515, nssv1865513
SamplesHGDP01284, HGDP00665, HGDP00998, HGDP00521, HGDP00778, HGDP01307, HGDP00542, HGDP01029, HGDP00456, HGDP00927
Known Genes
MethodSequencing
Analysislineage specific fixed duplications
PlatformNot reported
Comments
ReferenceSudmant_et_al_2013
Pubmed ID23825009
Accession Number(s)nsv948141
Frequency
Sample Size10
Observed Gain10
Observed Loss0
Observed Complex0
Frequencyn/a


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