A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5867932



Internal ID22642867
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr20:34217866..34219067hg38UCSC Ensembl
chr20:32805672..32806873hg19UCSC Ensembl
Cytoband20q11.22
Allele length
AssemblyAllele length
hg381202
hg191202
Variant TypeOTHER complex
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17485314
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nsv5867932
Frequency
Sample Size914
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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