A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5448597



Internal ID226867
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr3:142584991..142591947hg38UCSC Ensembl
chr3:142303833..142310789hg19UCSC Ensembl
Cytoband3q23
Allele length
AssemblyAllele length
hg386957
hg196957
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv16938884
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceByrska_Bishop_et_al_2022
Pubmed ID36055201
Accession Number(s)nsv5448597
Frequency
Sample Size3202
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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