A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5910314



Internal ID22685525
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr10:89347241..89363801hg38UCSC Ensembl
chr10:91106998..91123558hg19UCSC Ensembl
Cytoband10q23.31
Allele length
AssemblyAllele length
hg3816561
hg1916561
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17359460
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nsv5910314
Frequency
Sample Size914
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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