A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17727436



Internal ID151102
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr22:12386248..12396515hg38UCSC Ensembl
Cytoband
Allele length
AssemblyAllele length
hg3810268
Variant TypeCNV mobile element deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6147191
Supporting Variants
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceByrska_Bishop_et_al_2022
Pubmed ID36055201
Accession Number(s)nssv17727436
Frequency
Sample Size3202
Observed Gain0
Observed Loss1
Observed Complex0
Frequency0.001249


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