A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv948081



Internal ID18594927
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr10:79502678..79504045hg38UCSC Ensembl
Innerchr10:81262434..81263801hg19UCSC Ensembl
Innerchr10:80932440..80933807hg18UCSC Ensembl
Cytoband10q22.3
Allele length
AssemblyAllele length
hg381368
hg191368
hg181368
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv1857845, nssv1857851, nssv1857842, nssv1857848, nssv1857849, nssv1857847, nssv1857850, nssv1857844, nssv1857846, nssv1857843
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)nsv948081
Frequency
Sample Size10
Observed Gain10
Observed Loss0
Observed Complex0
Frequencyn/a


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