A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17480890



Internal ID22538794
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr21:41081514..41087615hg38UCSC Ensembl
chr21:42453441..42459542hg19UCSC Ensembl
Cytoband21q22.2
Allele length
AssemblyAllele length
hg386102
hg196102
Variant TypeOTHER copy number variation
Copy Number0
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5879914
Supporting Variants
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nssv17480890
Frequency
Sample Size914
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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