A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5558877



Internal ID331929
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr2:98764251..98764784hg38UCSC Ensembl
chr2:99380714..99381247hg19UCSC Ensembl
Cytoband2q11.2
Allele length
AssemblyAllele length
hg38534
hg19534
Variant TypeOTHER inversion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv16917553
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceByrska_Bishop_et_al_2022
Pubmed ID36055201
Accession Number(s)nsv5558877
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