A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17727656



Internal ID151322
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr22:19672727..19673540hg38UCSC Ensembl
chr22:19660250..19661063hg19UCSC Ensembl
Cytoband22q11.21
Allele length
AssemblyAllele length
hg38814
hg19814
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5544458
Supporting Variants
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceByrska_Bishop_et_al_2022
Pubmed ID36055201
Accession Number(s)nssv17727656
Frequency
Sample Size3202
Observed Gain0
Observed Loss1
Observed Complex0
Frequency0.000468


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