A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5997507



Internal ID21906850
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr4:52465294..52465346hg38UCSC Ensembl
chr4:53331460..53331512hg19UCSC Ensembl
Cytoband4q12
Allele length
AssemblyAllele length
hg3853
hg1953
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17547658
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceWu_et_al_2021
Pubmed ID34764282
Accession Number(s)nsv5997507
Frequency
Sample Size405
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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