A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv947918



Internal ID18248078
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr10:45863213..45894478hg38UCSC Ensembl
Innerchr10:46358661..46389926hg19UCSC Ensembl
Innerchr10:45678667..45709932hg18UCSC Ensembl
Cytoband10q11.21
Allele length
AssemblyAllele length
hg3831266
hg1931266
hg1831266
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv1846381, nssv1846385, nssv1846379, nssv1846378, nssv1846387, nssv1846384, nssv1846383, nssv1846386, nssv1846380, nssv1846382
SamplesHGDP00927, HGDP00778, HGDP00542, HGDP01029, HGDP01284, HGDP00521, HGDP00998, HGDP00456, HGDP01307, HGDP00665
Known Genes
MethodSequencing
Analysislineage specific fixed duplications
PlatformNot reported
Comments
ReferenceSudmant_et_al_2013
Pubmed ID23825009
Accession Number(s)nsv947918
Frequency
Sample Size10
Observed Gain10
Observed Loss0
Observed Complex0
Frequencyn/a


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