A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5407041



Internal ID186377
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr10:92472379..92472430hg38UCSC Ensembl
chr10:94232136..94232187hg19UCSC Ensembl
Cytoband10q23.33
Allele length
AssemblyAllele length
hg38279
hg19279
Variant TypeCNV alu insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17037897
Samples
Known GenesIDE
MethodSequencing
Analysis
Platform
Comments
ReferenceByrska_Bishop_et_al_2022
Pubmed ID36055201
Accession Number(s)nsv5407041
Frequency
Sample Size3202
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


Hosted by The Centre for Applied Genomics
Grant support for DGV
Please read the usage disclaimer