A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5540149



Internal ID314960
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr22:27830023..27830756hg38UCSC Ensembl
chr22:28226011..28226744hg19UCSC Ensembl
Cytoband22q12.1
Allele length
AssemblyAllele length
hg38734
hg19734
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17728266
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceByrska_Bishop_et_al_2022
Pubmed ID36055201
Accession Number(s)nsv5540149
Frequency
Sample Size3202
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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