A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5993758



Internal ID21903101
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr3:57968375..57991839hg38UCSC Ensembl
chr3:57954102..57977566hg19UCSC Ensembl
Cytoband3p14.3
Allele length
AssemblyAllele length
hg3823465
hg1923465
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17553213
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceWu_et_al_2021
Pubmed ID34764282
Accession Number(s)nsv5993758
Frequency
Sample Size405
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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