A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5505866



Internal ID282629
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr11:28179979..28208531hg38UCSC Ensembl
chr11:28201526..28230078hg19UCSC Ensembl
Cytoband11p14.1
Allele length
AssemblyAllele length
hg3828553
hg1928553
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17044506
Samples
Known GenesMETTL15
MethodSequencing
Analysis
Platform
Comments
ReferenceByrska_Bishop_et_al_2022
Pubmed ID36055201
Accession Number(s)nsv5505866
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