A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5463776



Internal ID241667
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr5:2039341..2066106hg38UCSC Ensembl
chr5:2039455..2066220hg19UCSC Ensembl
Cytoband5p15.33
Allele length
AssemblyAllele length
hg3826766
hg1926766
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv16960866
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceByrska_Bishop_et_al_2022
Pubmed ID36055201
Accession Number(s)nsv5463776
Frequency
Sample Size3202
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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