A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5569159



Internal ID21517514
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr3:45501801..45510565hg38UCSC Ensembl
chr3:45543293..45552057hg19UCSC Ensembl
Cytoband3p21.31
Allele length
AssemblyAllele length
hg388765
hg198765
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17130972
SamplesHG01114
Known GenesLARS2, LARS2-AS1
MethodMerging
Analysis
PlatformSee merged experiments
Comments
ReferenceEbert_et_al_2021
Pubmed ID33632895
Accession Number(s)nsv5569159
Frequency
Sample Size35
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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