A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17399182



Internal ID22457052
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr20:22619448..22620838hg38UCSC Ensembl
chr20:22600086..22601476hg19UCSC Ensembl
Cytoband20p11.21
Allele length
AssemblyAllele length
hg381391
hg191391
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5964821
Supporting Variants
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nssv17399182
Frequency
Sample Size914
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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