A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6015776



Internal ID21925119
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr5:108212085..108213925hg38UCSC Ensembl
chr5:107547786..107549626hg19UCSC Ensembl
Cytoband5q21.3
Allele length
AssemblyAllele length
hg381841
hg191841
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17540620
Samples
Known GenesFBXL17
MethodSequencing
Analysis
Platform
Comments
ReferenceWu_et_al_2021
Pubmed ID34764282
Accession Number(s)nsv6015776
Frequency
Sample Size405
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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