A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv3115092



Internal ID21298358
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr21:19020759..19025247hg38UCSC Ensembl
Innerchr21:20393078..20397566hg19UCSC Ensembl
Cytoband21q21.1
Allele length
AssemblyAllele length
hg384489
hg194489
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv14102555
Samplessample402
Known Genes
MethodOligo aCGH
Analysis
Platform
Comments
ReferenceLu_et_al_2017
Pubmed ID28705883
Accession Number(s)nsv3115092
Frequency
Sample Size467
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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