A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5867639



Internal ID22642574
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr21:42257791..42305062hg38UCSC Ensembl
chr21:43677901..43725172hg19UCSC Ensembl
Cytoband21q22.3
Allele length
AssemblyAllele length
hg3847272
hg1947272
Variant TypeOTHER complex
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17480895
Samples
Known GenesABCG1
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nsv5867639
Frequency
Sample Size914
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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