A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5993886



Internal ID21903229
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr3:62383448..62383516hg38UCSC Ensembl
chr3:62369123..62369191hg19UCSC Ensembl
Cytoband3p14.2
Allele length
AssemblyAllele length
hg3869
hg1969
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17537814
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceWu_et_al_2021
Pubmed ID34764282
Accession Number(s)nsv5993886
Frequency
Sample Size405
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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