A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv3114271



Internal ID21297537
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr21:39345837..39350987hg38UCSC Ensembl
Innerchr21:40717763..40722913hg19UCSC Ensembl
Cytoband21q22.2
Allele length
AssemblyAllele length
hg385151
hg195151
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv14101997
Samplessample189
Known GenesHMGN1
MethodOligo aCGH
Analysis
Platform
Comments
ReferenceLu_et_al_2017
Pubmed ID28705883
Accession Number(s)nsv3114271
Frequency
Sample Size467
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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