A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6012282



Internal ID21921625
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr7:5507648..5507945hg38UCSC Ensembl
chr7:5547279..5547576hg19UCSC Ensembl
Cytoband7p22.1
Allele length
AssemblyAllele length
hg38298
hg19298
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17577115
Samples
Known GenesFBXL18
MethodSequencing
Analysis
Platform
Comments
ReferenceWu_et_al_2021
Pubmed ID34764282
Accession Number(s)nsv6012282
Frequency
Sample Size405
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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