A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5933624



Internal ID22708938
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr13:107814772..107831153hg38UCSC Ensembl
chr13:108467120..108483501hg19UCSC Ensembl
Cytoband13q33.3
Allele length
AssemblyAllele length
hg3816382
hg1916382
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17350042
Samples
Known GenesFAM155A
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nsv5933624
Frequency
Sample Size914
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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