A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17392458



Internal ID22450328
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr21:42803922..42839868hg38UCSC Ensembl
chr21:44224032..44259978hg19UCSC Ensembl
Cytoband21q22.3
Allele length
AssemblyAllele length
hg3835947
hg1935947
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5957879
Supporting Variants
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nssv17392458
Frequency
Sample Size914
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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