A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5507116



Internal ID283845
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr11:93271197..93281784hg38UCSC Ensembl
chr11:93004363..93014950hg19UCSC Ensembl
Cytoband11q21
Allele length
AssemblyAllele length
hg3810588
hg1910588
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17052045
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceByrska_Bishop_et_al_2022
Pubmed ID36055201
Accession Number(s)nsv5507116
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