A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5516826



Internal ID293275
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr18:10220412..10225871hg38UCSC Ensembl
chr18:10220409..10225868hg19UCSC Ensembl
Cytoband18p11.22
Allele length
AssemblyAllele length
hg385460
hg195460
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17715370
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceByrska_Bishop_et_al_2022
Pubmed ID36055201
Accession Number(s)nsv5516826
Frequency
Sample Size3202
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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