A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5452546



Internal ID230698
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr4:11452156..11613152hg38UCSC Ensembl
chr4:11453780..11614776hg19UCSC Ensembl
Cytoband4p15.33
Allele length
AssemblyAllele length
hg38160997
hg19160997
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv16946855
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceByrska_Bishop_et_al_2022
Pubmed ID36055201
Accession Number(s)nsv5452546
Frequency
Sample Size3202
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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