A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5560337



Internal ID333347
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr3:5027267..5027434hg38UCSC Ensembl
chr3:5068952..5069119hg19UCSC Ensembl
Cytoband3p26.1
Allele length
AssemblyAllele length
hg38168
hg19168
Variant TypeOTHER sequence alteration
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv16929988
Samples
Known Genes
MethodSequencing
Analysis
Platform
Commentscomplex variant
ReferenceByrska_Bishop_et_al_2022
Pubmed ID36055201
Accession Number(s)nsv5560337
Frequency
Sample Size3202
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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