A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv14094418



Internal ID21290518
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr13:102578251..102583900hg38UCSC Ensembl
Innerchr13:103230601..103236250hg19UCSC Ensembl
Cytoband13q33.1
Allele length
AssemblyAllele length
hg385650
hg195650
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv3113483
Supporting Variants
Samplessample60
Known Genes
MethodOligo aCGH
Analysis
Platform
Comments
ReferenceLu_et_al_2017
Pubmed ID28705883
Accession Number(s)nssv14094418
Frequency
Sample Size467
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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