A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5550492



Internal ID324042
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr22:36461390..36461733hg38UCSC Ensembl
chr22:36857437..36857780hg19UCSC Ensembl
Cytoband22q12.3
Allele length
AssemblyAllele length
hg38344
hg19344
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17728781
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceByrska_Bishop_et_al_2022
Pubmed ID36055201
Accession Number(s)nsv5550492
Frequency
Sample Size3202
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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