A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv947931



Internal ID18248091
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr10:46397324..46414489hg38UCSC Ensembl
Innerchr10:47135259..47152438hg19UCSC Ensembl
Innerchr10:46555265..46572444hg18UCSC Ensembl
Cytoband10q11.22
Allele length
AssemblyAllele length
hg3817166
hg1917180
hg1817180
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv1844837, nssv1844843, nssv1844836, nssv1844835, nssv1844841, nssv1844838, nssv1844834, nssv1844840, nssv1844839, nssv1844842
SamplesHGDP00927, HGDP00778, HGDP00542, HGDP01029, HGDP01284, HGDP00521, HGDP00998, HGDP00456, HGDP01307, HGDP00665
Known GenesLINC00842
MethodSequencing
Analysislineage specific fixed duplications
PlatformNot reported
Comments
ReferenceSudmant_et_al_2013
Pubmed ID23825009
Accession Number(s)nsv947931
Frequency
Sample Size10
Observed Gain10
Observed Loss0
Observed Complex0
Frequencyn/a


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