A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv948078



Internal ID18248238
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr10:78035183..78036183hg38UCSC Ensembl
Innerchr10:79794941..79795941hg19UCSC Ensembl
Innerchr10:79464947..79465947hg18UCSC Ensembl
Cytoband10q22.3
Allele length
AssemblyAllele length
hg381001
hg191001
hg181001
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv1856828, nssv1856827, nssv1856825, nssv1856830, nssv1856831, nssv1856824, nssv1856833, nssv1856826, nssv1856829, nssv1856832
SamplesHGDP01284, HGDP00665, HGDP00998, HGDP00521, HGDP00778, HGDP01307, HGDP00542, HGDP01029, HGDP00456, HGDP00927
Known GenesRPS24
MethodSequencing
Analysislineage specific fixed duplications
PlatformNot reported
Comments
ReferenceSudmant_et_al_2013
Pubmed ID23825009
Accession Number(s)nsv948078
Frequency
Sample Size10
Observed Gain10
Observed Loss0
Observed Complex0
Frequencyn/a


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