A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5881116



Internal ID22656089
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr20:59045815..59047929hg38UCSC Ensembl
chr20:57620870..57622984hg19UCSC Ensembl
Cytoband20q13.32
Allele length
AssemblyAllele length
hg382115
hg192115
Variant TypeOTHER complex
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17486737
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nsv5881116
Frequency
Sample Size914
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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