A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv4444461



Internal ID22110641
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr14:39405879..39405879hg38UCSC Ensembl
chr14:39875083..39875083hg19UCSC Ensembl
Cytoband14q21.1
Allele length
AssemblyAllele length
hg382993
hg192993
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv15760683
Samples
Known GenesFBXO33
MethodSequencing
Analysis
Platform
CommentsSVTYPE=INS;REPTYPE=SUBSINS
ReferenceGenome_in_a_Bottle
Pubmed ID32541955
Accession Number(s)nsv4444461
Frequency
Sample Size1
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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