A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5982973



Internal ID21892316
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr1:240184922..240185220hg38UCSC Ensembl
chr1:240348222..240348520hg19UCSC Ensembl
Cytoband1q43
Allele length
AssemblyAllele length
hg38299
hg19299
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17519188
Samples
Known GenesFMN2
MethodSequencing
Analysis
Platform
Comments
ReferenceWu_et_al_2021
Pubmed ID34764282
Accession Number(s)nsv5982973
Frequency
Sample Size405
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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