A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv18071489



Internal ID20638529
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr21:41299239..41301827hg38UCSC Ensembl
chr21:42671166..42673754hg19UCSC Ensembl
Cytoband21q22.3
Allele length
AssemblyAllele length
hg382589
hg192589
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6547935
Supporting Variants
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nssv18071489
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequency0.00013


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