A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5580826



Internal ID21529320
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr3:26631671..26631908hg38UCSC Ensembl
chr3:26673162..26673399hg19UCSC Ensembl
Cytoband3p24.1
Allele length
AssemblyAllele length
hg38238
hg19238
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17133153
SamplesHG02587
Known GenesLRRC3B
MethodMerging
Analysis
PlatformSee merged experiments
Comments
ReferenceEbert_et_al_2021
Pubmed ID33632895
Accession Number(s)nsv5580826
Frequency
Sample Size35
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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