A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5558490



Internal ID331549
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr13:110033277..110033328hg38UCSC Ensembl
chr13:110685624..110685675hg19UCSC Ensembl
Cytoband13q34
Allele length
AssemblyAllele length
hg38462
hg19462
Variant TypeCNV line1 insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17694142
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceByrska_Bishop_et_al_2022
Pubmed ID36055201
Accession Number(s)nsv5558490
Frequency
Sample Size3202
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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