A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5948363



Internal ID22723847
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr22:36921117..36921332hg38UCSC Ensembl
chr22:37317159..37317374hg19UCSC Ensembl
Cytoband22q12.3
Allele length
AssemblyAllele length
hg38216
hg19216
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17403322
Samples
Known GenesCSF2RB
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nsv5948363
Frequency
Sample Size914
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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