A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5879803



Internal ID22654773
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr20:17646992..17648321hg38UCSC Ensembl
chr20:17627637..17628966hg19UCSC Ensembl
Cytoband20p12.1
Allele length
AssemblyAllele length
hg381330
hg191330
Variant TypeOTHER complex
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17483220
Samples
Known GenesRRBP1
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nsv5879803
Frequency
Sample Size914
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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