A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5868091



Internal ID22643026
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr20:23256492..23287726hg38UCSC Ensembl
chr20:23237129..23268363hg19UCSC Ensembl
Cytoband20p11.21
Allele length
AssemblyAllele length
hg3831235
hg1931235
Variant TypeOTHER complex
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17483304
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nsv5868091
Frequency
Sample Size914
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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