A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5501054



Internal ID277965
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr11:94374439..94390344hg38UCSC Ensembl
chr11:94107605..94123510hg19UCSC Ensembl
Cytoband11q21
Allele length
AssemblyAllele length
hg3815906
hg1915906
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17049986
Samples
Known GenesGPR83
MethodSequencing
Analysis
Platform
Comments
ReferenceByrska_Bishop_et_al_2022
Pubmed ID36055201
Accession Number(s)nsv5501054
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