A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5996489



Internal ID21905832
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr4:168893835..168903057hg38UCSC Ensembl
chr4:169814986..169824208hg19UCSC Ensembl
Cytoband4q32.3
Allele length
AssemblyAllele length
hg389223
hg199223
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17554745
Samples
Known GenesPALLD
MethodSequencing
Analysis
Platform
Comments
ReferenceWu_et_al_2021
Pubmed ID34764282
Accession Number(s)nsv5996489
Frequency
Sample Size405
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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