A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv948154



Internal ID18248314
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr10:96914584..96917068hg38UCSC Ensembl
Innerchr10:98674341..98676825hg19UCSC Ensembl
Innerchr10:98664331..98666815hg18UCSC Ensembl
Cytoband10q24.1
Allele length
AssemblyAllele length
hg382485
hg192485
hg182485
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv1863505, nssv1863511, nssv1863514, nssv1863506, nssv1863507, nssv1863510, nssv1863508, nssv1863509, nssv1863513, nssv1863512
SamplesHGDP01284, HGDP00665, HGDP00998, HGDP00521, HGDP00778, HGDP01307, HGDP00542, HGDP01029, HGDP00456, HGDP00927
Known GenesLCOR
MethodSequencing
Analysislineage specific fixed duplications
PlatformNot reported
Comments
ReferenceSudmant_et_al_2013
Pubmed ID23825009
Accession Number(s)nsv948154
Frequency
Sample Size10
Observed Gain10
Observed Loss0
Observed Complex0
Frequencyn/a


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