A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5440003



Internal ID218527
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr3:154520453..154526025hg38UCSC Ensembl
chr3:154238242..154243814hg19UCSC Ensembl
Cytoband3q25.2
Allele length
AssemblyAllele length
hg385573
hg195573
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv16940630
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceByrska_Bishop_et_al_2022
Pubmed ID36055201
Accession Number(s)nsv5440003
Frequency
Sample Size3202
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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