A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17407276



Internal ID22465146
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr20:32684407..32685292hg38UCSC Ensembl
chr20:31272209..31273094hg19UCSC Ensembl
Cytoband20q11.21
Allele length
AssemblyAllele length
hg38886
hg19886
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5956111
Supporting Variants
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nssv17407276
Frequency
Sample Size914
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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