A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5993750



Internal ID21903093
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr3:56719923..56720027hg38UCSC Ensembl
chr3:56753951..56754055hg19UCSC Ensembl
Cytoband3p14.3
Allele length
AssemblyAllele length
hg38105
hg19105
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17543263
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceWu_et_al_2021
Pubmed ID34764282
Accession Number(s)nsv5993750
Frequency
Sample Size405
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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