A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17728375



Internal ID152041
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr22:29586232..29587305hg38UCSC Ensembl
chr22:29982221..29983294hg19UCSC Ensembl
Cytoband22q12.2
Allele length
AssemblyAllele length
hg381074
hg191074
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5542442
Supporting Variants
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceByrska_Bishop_et_al_2022
Pubmed ID36055201
Accession Number(s)nssv17728375
Frequency
Sample Size3202
Observed Gain0
Observed Loss1
Observed Complex0
Frequency0.000156


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