A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5524226



Internal ID300435
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr18:73611937..73612397hg38UCSC Ensembl
chr18:71279172..71279632hg19UCSC Ensembl
Cytoband18q22.3
Allele length
AssemblyAllele length
hg38461
hg19461
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17719442
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceByrska_Bishop_et_al_2022
Pubmed ID36055201
Accession Number(s)nsv5524226
Frequency
Sample Size3202
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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