A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5455185



Internal ID233267
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr4:94383248..94389194hg38UCSC Ensembl
chr4:95304399..95310345hg19UCSC Ensembl
Cytoband4q22.3
Allele length
AssemblyAllele length
hg385947
hg195947
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv16951857
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceByrska_Bishop_et_al_2022
Pubmed ID36055201
Accession Number(s)nsv5455185
Frequency
Sample Size3202
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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