A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5557867



Internal ID330949
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr13:109541811..109545775hg38UCSC Ensembl
chr13:110194158..110198122hg19UCSC Ensembl
Cytoband13q33.3
Allele length
AssemblyAllele length
hg383965
hg193965
Variant TypeOTHER sequence alteration
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17694622
Samples
Known Genes
MethodSequencing
Analysis
Platform
Commentscomplex variant
ReferenceByrska_Bishop_et_al_2022
Pubmed ID36055201
Accession Number(s)nsv5557867
Frequency
Sample Size3202
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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