A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5509324



Internal ID285982
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr11:108802362..108822923hg38UCSC Ensembl
chr11:108673089..108693650hg19UCSC Ensembl
Cytoband11q22.3
Allele length
AssemblyAllele length
hg3820562
hg1920562
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17049157
Samples
Known GenesDDX10
MethodSequencing
Analysis
Platform
Comments
ReferenceByrska_Bishop_et_al_2022
Pubmed ID36055201
Accession Number(s)nsv5509324
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