A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5506615



Internal ID283355
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr13:61948168..62097963hg38UCSC Ensembl
chr13:62522301..62672096hg19UCSC Ensembl
Cytoband13q21.31
Allele length
AssemblyAllele length
hg38149796
hg19149796
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17691884
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceByrska_Bishop_et_al_2022
Pubmed ID36055201
Accession Number(s)nsv5506615
Frequency
Sample Size3202
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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