A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv14089059



Internal ID21291616
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr10:12263546..12276542hg38UCSC Ensembl
Innerchr10:12305545..12318541hg19UCSC Ensembl
Cytoband10p13
Allele length
AssemblyAllele length
hg3812997
hg1912997
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv3115618
Supporting Variants
Samplessample77
Known Genes
MethodOligo aCGH
Analysis
Platform
Comments
ReferenceLu_et_al_2017
Pubmed ID28705883
Accession Number(s)nssv14089059
Frequency
Sample Size467
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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