A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5589308



Internal ID21537871
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr21:42276682..42276756hg38UCSC Ensembl
chr21:43696792..43696866hg19UCSC Ensembl
Cytoband21q22.3
Allele length
AssemblyAllele length
hg3875
hg1975
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17119149
SamplesHG03125
Known GenesABCG1
MethodMerging
Analysis
PlatformSee merged experiments
Comments
ReferenceEbert_et_al_2021
Pubmed ID33632895
Accession Number(s)nsv5589308
Frequency
Sample Size35
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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