A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5880581



Internal ID22655551
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr20:20333443..20338052hg38UCSC Ensembl
chr20:20314087..20318696hg19UCSC Ensembl
Cytoband20p11.23
Allele length
AssemblyAllele length
hg384610
hg194610
Variant TypeOTHER complex
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17483254
Samples
Known GenesC20orf26
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nsv5880581
Frequency
Sample Size914
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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