A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5860687



Internal ID22635622
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr8:143307212..143321110hg38UCSC Ensembl
chr8:144389382..144403280hg19UCSC Ensembl
Cytoband8q24.3
Allele length
AssemblyAllele length
hg3813899
hg1913899
Variant TypeOTHER complex
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17507624
Samples
Known GenesTOP1MT
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nsv5860687
Frequency
Sample Size914
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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