A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5955908



Internal ID22731101
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr22:40957334..40957457hg38UCSC Ensembl
chr22:41353338..41353461hg19UCSC Ensembl
Cytoband22q13.2
Allele length
AssemblyAllele length
hg38124
hg19124
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17402916
Samples
Known GenesRBX1
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nsv5955908
Frequency
Sample Size914
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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