A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5541489



Internal ID316078
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr13:36142679..36142718hg38UCSC Ensembl
chr13:36716816..36716855hg19UCSC Ensembl
Cytoband13q13.3
Allele length
AssemblyAllele length
hg38293
hg19293
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17686885
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceByrska_Bishop_et_al_2022
Pubmed ID36055201
Accession Number(s)nsv5541489
Frequency
Sample Size3202
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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