A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5558379



Internal ID331444
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr1:25181390..25200719hg38UCSC Ensembl
chr1:25507881..25527210hg19UCSC Ensembl
Cytoband1p36.11
Allele length
AssemblyAllele length
hg3819330
hg1919330
Variant TypeOTHER inversion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv16900185
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceByrska_Bishop_et_al_2022
Pubmed ID36055201
Accession Number(s)nsv5558379
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