A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5908492



Internal ID22683702
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr11:59344998..59351628hg38UCSC Ensembl
chr11:59112471..59119101hg19UCSC Ensembl
Cytoband11q12.1
Allele length
AssemblyAllele length
hg386631
hg196631
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17358233
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nsv5908492
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