A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv947892



Internal ID18594739
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr10:42862785..42873481hg38UCSC Ensembl
Innerchr10:43358233..43368929hg19UCSC Ensembl
Innerchr10:42678239..42688935hg18UCSC Ensembl
Cytoband10q11.21
Allele length
AssemblyAllele length
hg3810697
hg1910697
hg1810697
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv1845051, nssv1845053, nssv1845056, nssv1845058, nssv1845055, nssv1845052, nssv1845049, nssv1845050, nssv1845057, nssv1845054
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)nsv947892
Frequency
Sample Size10
Observed Gain10
Observed Loss0
Observed Complex0
Frequencyn/a


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