A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5452887



Internal ID231029
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr3:9597385..9606557hg38UCSC Ensembl
chr3:9639069..9648241hg19UCSC Ensembl
Cytoband3p25.3
Allele length
AssemblyAllele length
hg389173
hg199173
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv16930836
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceByrska_Bishop_et_al_2022
Pubmed ID36055201
Accession Number(s)nsv5452887
Frequency
Sample Size3202
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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