A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17485314



Internal ID22543225
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr20:34217866..34219067hg38UCSC Ensembl
chr20:32805672..32806873hg19UCSC Ensembl
Cytoband20q11.22
Allele length
AssemblyAllele length
hg381202
hg191202
Variant TypeOTHER copy number variation
Copy Number0
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5867932
Supporting Variants
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nssv17485314
Frequency
Sample Size914
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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