A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5536226



Internal ID311732
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr22:37612261..37612568hg38UCSC Ensembl
chr22:38008268..38008575hg19UCSC Ensembl
Cytoband22q13.1
Allele length
AssemblyAllele length
hg38308
hg19308
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17728854
Samples
Known GenesGGA1
MethodSequencing
Analysis
Platform
Comments
ReferenceByrska_Bishop_et_al_2022
Pubmed ID36055201
Accession Number(s)nsv5536226
Frequency
Sample Size3202
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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