A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5880797



Internal ID22655767
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr20:32036722..32042164hg38UCSC Ensembl
chr20:30624525..30629967hg19UCSC Ensembl
Cytoband20q11.21
Allele length
AssemblyAllele length
hg385443
hg195443
Variant TypeOTHER complex
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17485293
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nsv5880797
Frequency
Sample Size914
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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