A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5555405



Internal ID328561
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr19:32878176..32959621hg38UCSC Ensembl
chr19:33369082..33450527hg19UCSC Ensembl
Cytoband19q13.11
Allele length
AssemblyAllele length
hg3881446
hg1981446
Variant TypeOTHER inversion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17722844
Samples
Known GenesCEP89
MethodSequencing
Analysis
Platform
Comments
ReferenceByrska_Bishop_et_al_2022
Pubmed ID36055201
Accession Number(s)nsv5555405
Frequency
Sample Size3202
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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