A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17355803



Internal ID22581472
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr11:92971063..92974705hg38UCSC Ensembl
chr11:92704229..92707871hg19UCSC Ensembl
Cytoband11q14.3
Allele length
AssemblyAllele length
hg383643
hg193643
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5920459
Supporting Variants
Samples
Known GenesMTNR1B
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nssv17355803
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