A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17403874



Internal ID22461744
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr22:50292636..50292741hg38UCSC Ensembl
chr22:50731065..50731170hg19UCSC Ensembl
Cytoband22q13.33
Allele length
AssemblyAllele length
hg38106
hg19106
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5947924
Supporting Variants
Samples
Known GenesPLXNB2
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nssv17403874
Frequency
Sample Size914
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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