A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17392726



Internal ID22450596
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr20:26612263..27461773hg38UCSC Ensembl
Cytoband
Allele length
AssemblyAllele length
hg38849511
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5958138
Supporting Variants
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nssv17392726
Frequency
Sample Size914
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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