A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5456222



Internal ID234290
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr4:46489501..46491790hg38UCSC Ensembl
chr4:46491518..46493807hg19UCSC Ensembl
Cytoband4p12
Allele length
AssemblyAllele length
hg382290
hg192290
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv16949935
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceByrska_Bishop_et_al_2022
Pubmed ID36055201
Accession Number(s)nsv5456222
Frequency
Sample Size3202
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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