A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv4441169



Internal ID22107349
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr4:15615448..15615448hg38UCSC Ensembl
chr4:15617071..15617071hg19UCSC Ensembl
Cytoband4p15.32
Allele length
AssemblyAllele length
hg38238
hg19238
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv15767050
Samples
Known GenesFBXL5
MethodSequencing
Analysis
Platform
CommentsSVTYPE=INS;REPTYPE=SIMPLEINS
ReferenceGenome_in_a_Bottle
Pubmed ID32541955
Accession Number(s)nsv4441169
Frequency
Sample Size1
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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