A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5560619



Internal ID333623
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr22:37817186..37817226hg38UCSC Ensembl
chr22:38213193..38213233hg19UCSC Ensembl
Cytoband22q13.1
Allele length
AssemblyAllele length
hg38801
hg19801
Variant TypeCNV sva insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17728876
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceByrska_Bishop_et_al_2022
Pubmed ID36055201
Accession Number(s)nsv5560619
Frequency
Sample Size3202
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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