A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5559289



Internal ID332327
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr8:101182252..101182259hg38UCSC Ensembl
chr8:102194480..102194487hg19UCSC Ensembl
Cytoband8q22.3
Allele length
AssemblyAllele length
hg388
hg198
Variant TypeOTHER sequence alteration
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17014759
Samples
Known Genes
MethodSequencing
Analysis
Platform
Commentscomplex variant
ReferenceByrska_Bishop_et_al_2022
Pubmed ID36055201
Accession Number(s)nsv5559289
Frequency
Sample Size3202
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


Hosted by The Centre for Applied Genomics
Grant support for DGV
Please read the usage disclaimer