A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv948159



Internal ID18595005
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr10:97478310..97480479hg38UCSC Ensembl
Innerchr10:99238067..99240236hg19UCSC Ensembl
Innerchr10:99228057..99230226hg18UCSC Ensembl
Cytoband10q24.1
Allele length
AssemblyAllele length
hg382170
hg192170
hg182170
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv1864959, nssv1864961, nssv1864966, nssv1864964, nssv1864960, nssv1864965, nssv1864963, nssv1864958, nssv1864957, nssv1864962
SamplesHGDP01284, HGDP00665, HGDP00998, HGDP00521, HGDP00778, HGDP01307, HGDP00542, HGDP01029, HGDP00456, HGDP00927
Known GenesMMS19
MethodSequencing
Analysislineage specific fixed duplications
PlatformNot reported
Comments
ReferenceSudmant_et_al_2013
Pubmed ID23825009
Accession Number(s)nsv948159
Frequency
Sample Size10
Observed Gain10
Observed Loss0
Observed Complex0
Frequencyn/a


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