A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17392394



Internal ID22450264
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr22:32565025..32565168hg38UCSC Ensembl
chr22:32961011..32961154hg19UCSC Ensembl
Cytoband22q12.3
Allele length
AssemblyAllele length
hg38144
hg19144
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5966498
Supporting Variants
Samples
Known GenesSYN3
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nssv17392394
Frequency
Sample Size914
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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