A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5966498



Internal ID22741433
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 StatusM
Merged Variants
Supporting Variantsnssv17392394
Samples
Known GenesSYN3
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nsv5966498
Frequency
Sample Size914
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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