A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5451292



Internal ID229478
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr3:40643999..40653886hg38UCSC Ensembl
chr3:40685490..40695377hg19UCSC Ensembl
Cytoband3p22.1
Allele length
AssemblyAllele length
hg389888
hg199888
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv16932316
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceByrska_Bishop_et_al_2022
Pubmed ID36055201
Accession Number(s)nsv5451292
Frequency
Sample Size3202
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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