A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17727673



Internal ID151339
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr22:19970188..19970245hg38UCSC Ensembl
chr22:19957711..19957768hg19UCSC Ensembl
Cytoband22q11.21
Allele length
AssemblyAllele length
hg3858
hg1958
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5547899
Supporting Variants
Samples
Known GenesARVCF
MethodSequencing
Analysis
Platform
Comments
ReferenceByrska_Bishop_et_al_2022
Pubmed ID36055201
Accession Number(s)nssv17727673
Frequency
Sample Size3202
Observed Gain0
Observed Loss1
Observed Complex0
Frequency0.000312


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