A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv3117337



Internal ID21300603
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr1:240020913..240135074hg38UCSC Ensembl
Innerchr1:240184213..240298374hg19UCSC Ensembl
Cytoband1q43
Allele length
AssemblyAllele length
hg38114162
hg19114162
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv14105377
Samplessample78
Known GenesFMN2
MethodOligo aCGH
Analysis
Platform
Comments
ReferenceLu_et_al_2017
Pubmed ID28705883
Accession Number(s)nsv3117337
Frequency
Sample Size467
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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