A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5926441



Internal ID22701668
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr11:79422013..79423347hg38UCSC Ensembl
chr11:79133057..79134391hg19UCSC Ensembl
Cytoband11q14.1
Allele length
AssemblyAllele length
hg381335
hg191335
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17362838
Samples
Known GenesMIR5579, TENM4
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nsv5926441
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