A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5554191



Internal ID327387
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr13:102762583..102762610hg38UCSC Ensembl
chr13:103414933..103414960hg19UCSC Ensembl
Cytoband13q33.1
Allele length
AssemblyAllele length
hg3863
hg1963
Variant TypeCNV line1 insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17692239
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceByrska_Bishop_et_al_2022
Pubmed ID36055201
Accession Number(s)nsv5554191
Frequency
Sample Size3202
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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