A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5491416



Internal ID268656
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr10:87828415..87828539hg38UCSC Ensembl
chr10:89588172..89588296hg19UCSC Ensembl
Cytoband10q23.31
Allele length
AssemblyAllele length
hg38125
hg19125
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17038394
Samples
Known GenesCFL1P1
MethodSequencing
Analysis
Platform
Comments
ReferenceByrska_Bishop_et_al_2022
Pubmed ID36055201
Accession Number(s)nsv5491416
Frequency
Sample Size3202
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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