A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5555608



Internal ID328761
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr9:87215627..87217313hg38UCSC Ensembl
chr9:89830542..89832228hg19UCSC Ensembl
Cytoband9q21.33
Allele length
AssemblyAllele length
hg381687
hg191687
Variant TypeOTHER sequence alteration
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17025438
Samples
Known Genes
MethodSequencing
Analysis
Platform
Commentscomplex variant
ReferenceByrska_Bishop_et_al_2022
Pubmed ID36055201
Accession Number(s)nsv5555608
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