A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv14088710



Internal ID21278749
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr10:129960567..129976883hg38UCSC Ensembl
Innerchr10:131758831..131775147hg19UCSC Ensembl
Cytoband10q26.3
Allele length
AssemblyAllele length
hg3816317
hg1916317
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv3117854
Supporting Variants
Samplessample273
Known GenesEBF3
MethodOligo aCGH
Analysis
Platform
Comments
ReferenceLu_et_al_2017
Pubmed ID28705883
Accession Number(s)nssv14088710
Frequency
Sample Size467
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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