A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5998869



Internal ID21908212
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr5:15567079..15567170hg38UCSC Ensembl
chr5:15567188..15567279hg19UCSC Ensembl
Cytoband5p15.1
Allele length
AssemblyAllele length
hg3892
hg1992
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17547833
Samples
Known GenesFBXL7
MethodSequencing
Analysis
Platform
Comments
ReferenceWu_et_al_2021
Pubmed ID34764282
Accession Number(s)nsv5998869
Frequency
Sample Size405
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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