A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5568892



Internal ID21517244
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr3:153022895..153022950hg38UCSC Ensembl
chr3:152740684..152740739hg19UCSC Ensembl
Cytoband3q25.2
Allele length
AssemblyAllele length
hg3856
hg1956
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17121713
SamplesNA19983
Known Genes
MethodMerging
Analysis
PlatformSee merged experiments
Comments
ReferenceEbert_et_al_2021
Pubmed ID33632895
Accession Number(s)nsv5568892
Frequency
Sample Size35
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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