A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5996221



Internal ID21905564
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr4:160261175..160263753hg38UCSC Ensembl
chr4:161182327..161184905hg19UCSC Ensembl
Cytoband4q32.1
Allele length
AssemblyAllele length
hg382579
hg192579
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17557265
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceWu_et_al_2021
Pubmed ID34764282
Accession Number(s)nsv5996221
Frequency
Sample Size405
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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