A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5993312



Internal ID21902655
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr3:28412235..28426791hg38UCSC Ensembl
chr3:28453726..28468282hg19UCSC Ensembl
Cytoband3p24.1
Allele length
AssemblyAllele length
hg3814557
hg1914557
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17543948
Samples
Known GenesZCWPW2
MethodSequencing
Analysis
Platform
Comments
ReferenceWu_et_al_2021
Pubmed ID34764282
Accession Number(s)nsv5993312
Frequency
Sample Size405
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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