A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5526452



Internal ID302582
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr18:36270035..36276733hg38UCSC Ensembl
chr18:33849998..33856696hg19UCSC Ensembl
Cytoband18q12.2
Allele length
AssemblyAllele length
hg386699
hg196699
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17717357
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceByrska_Bishop_et_al_2022
Pubmed ID36055201
Accession Number(s)nsv5526452
Frequency
Sample Size3202
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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