A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv948063



Internal ID18248223
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr10:72914686..72924268hg38UCSC Ensembl
Innerchr10:74674444..74684026hg19UCSC Ensembl
Innerchr10:74344450..74354032hg18UCSC Ensembl
Cytoband10q22.1
Allele length
AssemblyAllele length
hg389583
hg199583
hg189583
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv1857475, nssv1857470, nssv1857474, nssv1857466, nssv1857473, nssv1857468, nssv1857467, nssv1857472, nssv1857469, nssv1857471
SamplesHGDP00927, HGDP00778, HGDP00542, HGDP01029, HGDP01284, HGDP00521, HGDP00998, HGDP00456, HGDP01307, HGDP00665
Known GenesOIT3
MethodSequencing
Analysislineage specific fixed duplications
PlatformNot reported
Comments
ReferenceSudmant_et_al_2013
Pubmed ID23825009
Accession Number(s)nsv948063
Frequency
Sample Size10
Observed Gain10
Observed Loss0
Observed Complex0
Frequencyn/a


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