A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv3114185



Internal ID21297451
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr21:14239074..14241621hg38UCSC Ensembl
Innerchr21:15611395..15613942hg19UCSC Ensembl
Cytoband21q11.2
Allele length
AssemblyAllele length
hg382548
hg192548
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv14101988
Samplessample181
Known Genes
MethodOligo aCGH
Analysis
Platform
Comments
ReferenceLu_et_al_2017
Pubmed ID28705883
Accession Number(s)nsv3114185
Frequency
Sample Size467
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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