A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17408814



Internal ID22466684
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr20:26354101..28213385hg38UCSC Ensembl
Cytoband
Allele length
AssemblyAllele length
hg381859285
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5952311
Supporting Variants
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nssv17408814
Frequency
Sample Size914
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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