A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5994598



Internal ID21903941
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr4:108676999..108677478hg38UCSC Ensembl
chr4:109598155..109598634hg19UCSC Ensembl
Cytoband4q25
Allele length
AssemblyAllele length
hg38480
hg19480
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17550283
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceWu_et_al_2021
Pubmed ID34764282
Accession Number(s)nsv5994598
Frequency
Sample Size405
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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