A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5881716



Internal ID22656692
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr20:36057663..36059592hg38UCSC Ensembl
chr20:34645585..34647514hg19UCSC Ensembl
Cytoband20q11.23
Allele length
AssemblyAllele length
hg381930
hg191930
Variant TypeOTHER complex
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17485355
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nsv5881716
Frequency
Sample Size914
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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