A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5482933



Internal ID260378
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr10:88720097..88721828hg38UCSC Ensembl
chr10:90479854..90481585hg19UCSC Ensembl
Cytoband10q23.31
Allele length
AssemblyAllele length
hg381732
hg191732
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17049556
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceByrska_Bishop_et_al_2022
Pubmed ID36055201
Accession Number(s)nsv5482933
Frequency
Sample Size3202
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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