A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv948191



Internal ID18595037
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr10:114118510..114119115hg38UCSC Ensembl
Innerchr10:115878269..115878874hg19UCSC Ensembl
Innerchr10:115868259..115868864hg18UCSC Ensembl
Cytoband10q25.3
Allele length
AssemblyAllele length
hg38606
hg19606
hg18606
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv1868515, nssv1868506, nssv1868513, nssv1868510, nssv1868509, nssv1868512, nssv1868511, nssv1868508, nssv1868514, nssv1868507
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)nsv948191
Frequency
Sample Size10
Observed Gain10
Observed Loss0
Observed Complex0
Frequencyn/a


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