A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5446847



Internal ID225164
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr4:15636535..15638507hg38UCSC Ensembl
chr4:15638158..15640130hg19UCSC Ensembl
Cytoband4p15.32
Allele length
AssemblyAllele length
hg381973
hg191973
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv16945236
Samples
Known GenesFBXL5
MethodSequencing
Analysis
Platform
Comments
ReferenceByrska_Bishop_et_al_2022
Pubmed ID36055201
Accession Number(s)nsv5446847
Frequency
Sample Size3202
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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