A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6058489



Internal ID21967722
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr1:157760751..157760751hg38UCSC Ensembl
chr1:157730541..157730541hg19UCSC Ensembl
Cytoband1q23.1
Allele length
AssemblyAllele length
hg38125
hg19125
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17531006
Samples
Known GenesFCRL2
MethodSequencing
Analysis
Platform
Comments
ReferenceWu_et_al_2021
Pubmed ID34764282
Accession Number(s)nsv6058489
Frequency
Sample Size405
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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