A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5453337



Internal ID231461
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr3:137022432..137024596hg38UCSC Ensembl
chr3:136741274..136743438hg19UCSC Ensembl
Cytoband3q22.3
Allele length
AssemblyAllele length
hg382165
hg192165
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv16939347
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceByrska_Bishop_et_al_2022
Pubmed ID36055201
Accession Number(s)nsv5453337
Frequency
Sample Size3202
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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