A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv948060



Internal ID18594906
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr10:70786763..70803864hg38UCSC Ensembl
Innerchr10:72546519..72563620hg19UCSC Ensembl
Innerchr10:72216525..72233626hg18UCSC Ensembl
Cytoband10q22.1
Allele length
AssemblyAllele length
hg3817102
hg1917102
hg1817102
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv1857263, nssv1857262, nssv1857257, nssv1857258, nssv1857256, nssv1857255, nssv1857261, nssv1857259, nssv1857260, nssv1857264
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)nsv948060
Frequency
Sample Size10
Observed Gain10
Observed Loss0
Observed Complex0
Frequencyn/a


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