A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17728983



Internal ID152649
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr22:39057564..39069700hg38UCSC Ensembl
chr22:39453569..39465705hg19UCSC Ensembl
Cytoband22q13.1
Allele length
AssemblyAllele length
hg3812137
hg1912137
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5540871
Supporting Variants
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceByrska_Bishop_et_al_2022
Pubmed ID36055201
Accession Number(s)nssv17728983
Frequency
Sample Size3202
Observed Gain0
Observed Loss1
Observed Complex0
Frequency0.000156


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