A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5962155



Internal ID22737091
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr22:31269916..31269977hg38UCSC Ensembl
chr22:31665902..31665963hg19UCSC Ensembl
Cytoband22q12.2
Allele length
AssemblyAllele length
hg3862
hg1962
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17393651
Samples
Known GenesLIMK2
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nsv5962155
Frequency
Sample Size914
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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