A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5670794



Internal ID21619099
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr10:87308006..87425030hg38UCSC Ensembl
chr10:89067763..89184787hg19UCSC Ensembl
Cytoband10q23.2
Allele length
AssemblyAllele length
hg38117025
hg19117025
Variant TypeOTHER inversion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17072215
SamplesHG02818
Known GenesLINC00864, LOC439994, NUTM2A-AS1, NUTM2D
MethodMerging
Analysis
PlatformSee merged experiments
Comments
ReferenceEbert_et_al_2021
Pubmed ID33632895
Accession Number(s)nsv5670794
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