A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17728896



Internal ID152562
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr22:38003428..38003778hg38UCSC Ensembl
chr22:38399435..38399785hg19UCSC Ensembl
Cytoband22q13.1
Allele length
AssemblyAllele length
hg38351
hg19351
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5537029
Supporting Variants
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceByrska_Bishop_et_al_2022
Pubmed ID36055201
Accession Number(s)nssv17728896
Frequency
Sample Size3202
Observed Gain0
Observed Loss1
Observed Complex0
Frequency0.000156


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