A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5920459



Internal ID22695682
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 StatusM
Merged Variants
Supporting Variantsnssv17355803
Samples
Known GenesMTNR1B
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nsv5920459
Frequency
Sample Size914
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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