A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5872592



Internal ID22647532
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr20:390256..396655hg38UCSC Ensembl
chr20:370900..377299hg19UCSC Ensembl
Cytoband20p13
Allele length
AssemblyAllele length
hg386400
hg196400
Variant TypeOTHER complex
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17485958
Samples
Known GenesTRIB3
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nsv5872592
Frequency
Sample Size914
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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