A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5866728



Internal ID22641663
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr13:107814820..107828693hg38UCSC Ensembl
chr13:108467168..108481041hg19UCSC Ensembl
Cytoband13q33.3
Allele length
AssemblyAllele length
hg3813874
hg1913874
Variant TypeOTHER complex
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17460508
Samples
Known GenesFAM155A
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nsv5866728
Frequency
Sample Size914
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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