A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv1857469



Internal ID17481873
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr10:72914686..72924268hg38UCSC Ensembl
Innerchr10:74674444..74684026hg19UCSC Ensembl
Innerchr10:74344450..74354032hg18UCSC Ensembl
Cytoband10q22.1
Allele length
AssemblyAllele length
hg389583
hg199583
hg189583
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv948063
Supporting Variants
SamplesHGDP00998
Known GenesOIT3
MethodSequencing
Analysislineage specific fixed duplications
PlatformNot reported
Commentslineage specific duplication - fixed_Pab-Ppy-Ggod-Ggog-Gbeg-Ptrs-Ptrt-Ptre-Ptrv-Ppa-Hsa-Hde
ReferenceSudmant_et_al_2013
Pubmed ID23825009
Accession Number(s)nssv1857469
Frequency
Sample Size10
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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