A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5879029



Internal ID22653996
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr21:45299449..45332311hg38UCSC Ensembl
chr21:46719364..46752226hg19UCSC Ensembl
Cytoband21q22.3
Allele length
AssemblyAllele length
hg3832863
hg1932863
Variant TypeOTHER complex
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17480926
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nsv5879029
Frequency
Sample Size914
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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