A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5672408



Internal ID21620713
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr18:10002..112429hg38UCSC Ensembl
chr18:10002..112429hg19UCSC Ensembl
Cytoband18p11.32
Allele length
AssemblyAllele length
hg38102428
hg19102428
Variant TypeOTHER inversion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17100097
SamplesHG03125
Known GenesMIR8078, ROCK1P1
MethodMerging
Analysis
PlatformSee merged experiments
Comments
ReferenceEbert_et_al_2021
Pubmed ID33632895
Accession Number(s)nsv5672408
Frequency
Sample Size35
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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