A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5408666



Internal ID187990
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr5:14687843..14687894hg38UCSC Ensembl
chr5:14687952..14688003hg19UCSC Ensembl
Cytoband5p15.2
Allele length
AssemblyAllele length
hg38278
hg19278
Variant TypeCNV alu insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv16962690
Samples
Known GenesFAM105B
MethodSequencing
Analysis
Platform
Comments
ReferenceByrska_Bishop_et_al_2022
Pubmed ID36055201
Accession Number(s)nsv5408666
Frequency
Sample Size3202
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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