A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5871863



Internal ID22646801
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr20:355166..357715hg38UCSC Ensembl
chr20:335810..338359hg19UCSC Ensembl
Cytoband20p13
Allele length
AssemblyAllele length
hg382550
hg192550
Variant TypeOTHER complex
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17485334
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nsv5871863
Frequency
Sample Size914
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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