A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5560953



Internal ID333945
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr13:45312294..45312554hg38UCSC Ensembl
chr13:45886429..45886689hg19UCSC Ensembl
Cytoband13q14.13
Allele length
AssemblyAllele length
hg38261
hg19261
Variant TypeOTHER inversion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17687396
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceByrska_Bishop_et_al_2022
Pubmed ID36055201
Accession Number(s)nsv5560953
Frequency
Sample Size3202
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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